Articles
Articles are a collaborative effort to provide a single canonical page on all topics relevant to the practice of radiology. As such, articles are written and edited by countless contributing members over a period of time. A global group of dedicated editors oversee accuracy, consulting with expert advisers, and constantly reviewing additions.
785 results found
Article
Acrania
Acrania is a rare lethal congenital anomaly characterized by an absence of the calvaria.
Epidemiology
The estimated incidence is at ~1:1000 pregnancies 4.
Pathology
The condition is thought to result from abnormal migration of mesenchymal tissue, which normally covers the cerebral hemispher...
Article
Birth trauma
Birth trauma (a.k.a. birth injury) relates to those conditions caused by both physical/mechanical and hypoxic injuries.
Epidemiology
Birth trauma occurs in ~5 per 1000 births 2.
Risk factors
asphyxia
breech presentation
shoulder dystocia
instrument delivery
macrosomia
obstructed labor
...
Article
Preterm premature rupture of membranes
Preterm premature rupture of membranes (PPROM) refers to rupture of membranes prior to 37 weeks of gestation.
Epidemiology
It is thought to occur in 0.4-2% of all pregnancies. It however may account for up to one-third of all preterm births (particularly in the United States 5).
Pathology
PP...
Article
Placental chorioangioma
Placental chorioangiomas are benign vascular tumors of placental origin. It is the most common tumor of the placenta and is usually found incidentally.
Epidemiology
The estimated incidence is at ~1% of all pregnancies 3.
Associations
Recognized associations include:
hydrops fetalis: also li...
Article
Noonan syndrome
Noonan syndrome (NS) is a genetically and phenotypically heterogeneous non-aneuploidic congenital RASopathy. Affected individuals can bear some clinical features similar to that of Turner syndrome.
Epidemiology
The estimated incidence is at ~1 in 1000-2500 10. As individuals have normal numbe...
Article
Fetal macrosomia
Fetal macrosomia, also sometimes termed large for gestational age (LGA), is usually defined when the estimated fetal weight (EFW) is greater than the 90th percentile. According to this definition, it affects up to 10% of all live births. Some also use an increased birth weight (i.e. >4500 g) in ...
Article
Limb body wall complex
The limb-body wall complex (LBWC) is a rare variable group of congenital limb and body wall defects (involving mainly the chest and abdomen). They can include:
abdominoschisis: usually large and left-sided 4, and almost always present
thoracic wall defect / thoracoschisis
ectopia cordis
anom...
Article
Cleft lip and palate
Cleft lip and palate is one of the commonest neonatal facial anomalies. In ~80% of cases, the two features tend to occur together 6.
Epidemiology
It is estimated to occur with an incidence of ~1 in 700-1000 live births 1. This can increase to 4% for a sibling of a previously affected fetus and...
Article
Twin reversed arterial perfusion
Twin reversed arterial perfusion (TRAP) sequence is a rare complication of monochorionic pregnancies. It develops when the following conditions are present:
1. lack of a well-formed heart in one of the twins (so-called acardiac twin), and
2. a superficial artery to artery placental anastomosis...
Article
Hysterosalpingogram
A hysterosalpingogram (HSG) is a fluoroscopic examination of the uterus and the fallopian tubes, most commonly used in the investigation of infertility or recurrent spontaneous abortions.
Indications
infertility: to assess uterine morphology and tubal patency
Contraindications
pregnancy
act...
Article
Polydactyly
Polydactyly (less commonly called hyperdactyly) refers to the situation where there are more than the usual number of digits (five) in a hand or foot. It can be broadly classified as:
preaxial polydactyly: extra digit(s) towards the thumb/hallux (radially)
postaxial polydactyly: extra digit(s)...
Article
Amniotic band syndrome
Amniotic band syndrome (ABS) comprises a wide spectrum of abnormalities, all of which result from entrapment of various fetal body parts in a disrupted amnion. Due to the randomness of entrapment, each affected individual has the potential to form a unique deficit.
Epidemiology
The phenomenon ...
Article
Single umbilical artery
Single umbilical artery is a congenital absence of either the right or left umbilical artery. In the usual situation, there are paired umbilical arteries. For unknown reasons, the absence of the left umbilical artery is much more common (~70%).
Epidemiology
The estimated prevalence is ~0.4-1% ...
Article
Radial ray anomaly
Radial ray anomalies comprise of a large spectrum of upper limb anomalies which range from partial (radial hypoplasia) to a complete (radial aplasia) deficiency of the radius with or without accompanying deficiency of the thumb bones.
Pathology
Associations
They can be associated with a numbe...
Article
Haematometrium
A haematometrium refers to retention of blood into the endometrial cavity due to obstruction at the level of the uterus, cervix, or vagina.
Primary haematometrium occurs in young women, usually due to congenital anomalies such as an imperforate hymen or a non-communicating Müllerian duct. Secon...
Article
Echogenic intracardiac focus
Echogenic intracardiac focus (EIF) is a relatively common sonographic observation that may be present on an antenatal ultrasound scan.
Epidemiology
They are thought to be present in ~4-5% of karyotypically normal fetuses. They may be more common in the Asian population 5.
Associations
trisom...
Article
Congenital talipes equinovarus
Congenital talipes equinovarus is considered the most common anomaly affecting the feet diagnosed on antenatal ultrasound.
Terminology
While some use talipes equinovarus and clubfoot synonymously, in certain publications, the term clubfoot is considered a more general descriptive term that des...
Article
Intrauterine growth restriction
Intrauterine growth restriction (IUGR) or fetal growth restriction (FGR) is defined as an estimated fetal weight (EFW) and/or abdominal circumference (AC) at one point in time during pregnancy being below 3rd percentile or EFW and/or AC below the 10th percentile for gestational age with derange...
Article
Fetal echocardiography views
A standard fetal echocardiogram consists of several specific views which can be obtained to optimize visualization of different structures and anomalies. They include:
Basic views
abdominal situs view / transverse view of abdomen
four chamber view
left ventricular outflow tract ...
Article
Birth fracture of the clavicle
Birth fractures of the clavicle occur in 0.5-1% of vaginal deliveries and are the most frequent birth-related fracture. They are most commonly seen following normal, uncomplicated births but there is recognized increased incidence with high birth weight babies, forceps delivery and shoulder dyst...
Article
Iniencephaly
Iniencephaly is a rare neural tube defect resulting in the following features 1,2:
occipital bone defect
partial or total absence (rachischisis) of cervicothoracic vertebrae
fixed fetal head retroflexion
Epidemiology
The estimated incidence is at ~0.1-10 per 10,000 live births 5. There is...
Article
Choroid plexus cyst (antenatal)
Antenatal choroid plexus cysts are benign and are often transient typically resulting in utero from an infolding of the neuroepithelium.
They should not be confused with adult choroid plexus cysts (which are very commonly found at autopsy and likely degenerative), large intraventricular simpl...
Article
Apert syndrome
Apert syndrome (also known as type I acrocephalosyndactyly) is a syndrome that is predominantly characterized by skull and limb malformations.
Epidemiology
The estimated incidence is 1 case per 65-80,000 pregnancies.
Risk factors
increased paternal age has been proposed 6
Associations
CNS ...
Article
Abnormally eccentric gestational sac
An eccentrically-located gestational sac towards the fundus of the uterus is the normal sonographic appearance, however, an abnormally eccentric gestational sac on ultrasound may be apparent due to a number of causes:
interstitial ectopic pregnancy 1
normally implanted pregnancy in a
bicornu...
Article
Cephalocele
Cephalocele refers to the outward herniation of CNS contents through a defect in the cranium. The vast majority are midline.
Epidemiology
The estimated incidence is 0.8-4:10,000 live births 13 with a well recognized geographical variation between types; however, this has been speculated to be ...
Article
Circumvallate placenta
Circumvallate placenta refers to a variation in placental morphology in which, as a result of a small chorionic plate, the amnion and chorion fetal membranes ‘double back’ around the edge of the placenta.
Epidemiology
The prevalence is estimated to be around 1-7% 3.
Pathology
There is an inw...
Article
Hydrops fetalis
Hydrops fetalis is excessive extravasation of fluid into the third space in a fetus which could be due to heart failure, volume overload, decreased oncotic pressure, or increased vascular permeability. Hydrops is defined as the accumulation of fluid +/- edema involving at least two fetal compone...
Article
Fetal conditions associated with maternal diabetes
There are numerous fetal congenital anomalies associated with maternal diabetes.
They include
cardiac: congenital cardiac anomalies
ventricular septal defect (VSD) 5
conotruncal anomalies
transposition of the great arteries (TGA)
truncus arteriosus
fetal congestive cardiac failure (witho...
Article
Corpus luteum
The corpus luteum (plural: corpora lutea) is a temporary endocrine structure involved in ovulation and early pregnancy.
During ovulation, the primary follicle forms the secondary follicle and subsequently the mature vesicular follicle.
At ovulation the follicle ruptures expelling the ovum into...
Article
Failed early pregnancy
Failed early pregnancy (sometimes termed embryonic demise) refers to the death of the embryo and therefore, miscarriage. The most common cause of embryonic death is a chromosomal abnormality.
Radiographic features
Ultrasound
Findings diagnostic of pregnancy failure
crown-rump length (CRL)...
Article
Skeletal dysplasia
Skeletal dysplasia (also known as osteochondrodysplasia) refers to any abnormality in bone formation. There is a very wide clinicopathological spectrum and any part of the skeleton can be affected.
Epidemiology
The overall prevalence is estimated at ~2 per 10,000 live births 3.
Pathology
Typ...
Article
Rhizomelic dwarfism
Rhizomelic dwarfism is a type of dwarfism where the dominant feature is proximal (i.e. femoral and humeral) limb shortening.
Epidemiology
Associations
certain types of atelosteogenesis
diastrophic dysplasia
kyphomelic dysplasias
Pathology
Classification
The following conditions fall unde...
Article
Fetal tumors
Although rare, a number of tumors may be diagnosed antenatally. These fetal tumors are a diverse and a unique group of conditions, and include:
neuroblastoma: most common tumor overall
teratomas
sacrococcygeal teratoma
head and neck teratoma/epignathus
mediastinal teratoma
intrapericardial...
Article
Syntelencephaly
Syntelencephaly, also known as middle interhemispheric variant (MIHV), is a mild subtype of holoprosencephaly that is characterized by an abnormal midline connection of the cerebral hemispheres between the posterior frontal and parietal regions.
Epidemiology
Syntelencephaly is a congenital ma...
Article
Currarino syndrome
The Currarino syndrome is a complex condition variably comprised of characteristic congenital anomalies of the sacrum, anorectum and presacral soft tissues. It is also known as the Currarino triad or ASP triad, however, not all three features are always present 6.
anorectal malformation or ...
Article
Sacrococcygeal teratoma
Sacrococcygeal teratoma refers to a teratoma arising in the sacrococcygeal region. The coccyx is almost always involved 6.
Epidemiology
It is the most common congenital tumor in fetus 11 and neonate 3. The incidence is estimated at ~1:35,000-40,000. There is a recognized female predilection wi...
Article
Meckel-Gruber syndrome
Meckel-Gruber syndrome (MGS) is classically characterized by the triad of:
renal cystic dysplasia: multiple renal cysts (present in most cases)
occipital encephalocele / holoprosencephaly (~70%)
postaxial polydactyly: usually hexadactyly (~65%)
Additional hepatic developmental defects and he...
Article
Hydranencephaly
Hydranencephaly is a rare encephalopathy that occurs in-utero. It is characterized by destruction of the cerebral hemispheres which are transformed into a membranous sac containing cerebrospinal fluid and the remnants of cortex and white matter 1.
Porencephaly is considered a less severe degree...
Article
Endometrial thickness
Endometrial thickness is a commonly measured parameter on routine gynecological ultrasound and MRI. The appearance, as well as the thickness of the endometrium, will depend on whether the patient is of reproductive age or postmenopausal and, if of reproductive age, at what point in the menstrual...
Article
Placenta accreta spectrum disorders
Placenta accreta spectrum (PAS) disorders describe the degree to which there is an invasion by chorionic villi into the myometrium because of a defect in the decidua basalis.
Epidemiology
placenta accreta:
the commonest type of placental invasion (~75% of cases)
occurs in ~1 in 7000 pregnanc...
Article
Pentalogy of Cantrell
The pentalogy of Cantrell is an extremely rare phenomenon with an incidence estimated at around 6 per million live births 3.
It encompasses the following 5 main features 1.
omphalocele
ectopia cordis (abnormal location of heart)
diaphragmatic defect
pericardial defect or sternal cleft
car...
Article
Neural tube defects
Neural tube defect (NTD) refers to the incomplete closure of the neural tube in very early pregnancy, resulting in cranial defects or spinal dysraphism.
The neural tube comprises a bundle of nerve sheath which closes to form brain caudally and spinal cord rostrally. The closure should occur at ...
Article
Esophageal atresia
Esophageal atresia refers to an absence in the continuity of the esophagus due to an inappropriate division of the primitive foregut into the trachea and esophagus. This is the most common congenital anomaly of the esophagus.
Epidemiology
It is thought to occur in ~1:3000-4500 live births 3.
...
Article
Cornelia de Lange syndrome
Cornelia de Lange syndrome (CdLS) is an extremely rare clinically heterogeneous developmental disorder of unknown etiology. Although the described clinical symptomatology is very broad, the majority of cases include growth impairment, learning disability and dysmorphic facies.
Epidemiology
The...
Article
Renal agenesis
Renal agenesis refers to a congenital absence of one or both kidneys. If bilateral (traditionally known as the classic Potter syndrome) the condition is fatal, whereas if unilateral, patients can have a normal life expectancy.
Epidemiology
Unilateral renal agenesis affects approximately 1 in ...
Article
Cardiac rhabdomyoma
Cardiac rhabdomyomas are a type of benign myocardial tumor and are considered the most common fetal cardiac tumor. They have a strong association with tuberous sclerosis.
Epidemiology
Cardiac rhabdomyomas are often multiple and can represent up to 90% of cardiac tumors in the pediatric populat...
Article
Pseudodysraphism
A pseudodysraphism refers to the splayed appearance of a normal spine created due to excessive craniocaudal angulation during sonographic evaluation. This can erroneously lead to the diagnosis of a spinal neural tube defect.
Article
Anencephaly
Anencephaly is the most severe form of cranial neural tube defect and is characterized by an absence of cortical tissue (although the brainstem and cerebellum may be variably present) as well as an absence of the cranial vault. The morphological spectrum within anencephaly ranges from holocrania...
Article
Fetal heart beat
Fetal heart beat can be detected as early as 34 days (just under 6 weeks) gestation on good quality, high frequency transvaginal ultrasound, as a crown rump length (CRL) of as little as 1-2 mm.
If a fetal heartbeat cannot be identified with a CRL ≥7 mm using transvaginal scanning, then embryona...
Article
Yolk sac
Yolk sac is the first anatomical structure identified within the gestational sac. It plays a critical role in embryonal development by providing nutrients, serving as the site of initial hematopoiesis, providing endocrine, metabolic and immunological functions and contributing to the development...
Article
Double bleb sign
A double bleb sign is a sonographic feature where there is visualization of a gestational sac containing a yolk sac and amniotic sac giving an appearance of two small bubbles 2. The embryonic disc is located between the two bubbles. It is an important feature of an intrauterine pregnancy and thu...
Article
First trimester
The first trimester is defined as the first 13 weeks of pregnancy following the last normal menstrual period (some authors refer to early pregnancy as 0-10 weeks). It can be divided into a number of phases, each of which has typical clinical issues. These phases are:
conceptus phase: 3-5 weeks
...
Article
Intradecidual sac sign
Intradecidual sac sign (IDSS) is a useful feature in identifying an early intrauterine pregnancy (IUP) as early as 25 days of gestation1. The threshold level (earliest one can see the sign) is 24 days of gestation and the discriminatory level (one should always see the sac) is 47 days. As per th...
Article
Ventricular septal defect
Ventricular septal defects (VSD) represent a hole or pathway in the interventricular septum that allows for communication between the right and left ventricles. It typically results in a left-to-right shunt.
Epidemiology
They represent one of the most common congenital cardiac anomalies and ma...
Article
Thanatophoric dysplasia
Thanatophoric dysplasia is a lethal skeletal dysplasia. It is the most common lethal skeletal dysplasia followed by osteogenesis imperfecta type II.
Epidemiology
The estimated incidence is around 1:25,000-50,000 3.
Associations
polyhydramnios 4
Pathology
Subtypes
There are two recognized...
Article
Missed miscarriage
A missed miscarriage, sometimes termed a missed abortion 3, is a situation when there is a non-viable fetus within the uterus, without symptoms of a miscarriage.
Radiographic features
Ultrasound
Ultrasound diagnosis of miscarriage should only be considered when either a mean gestation sac d...
Article
Semilobar holoprosencephaly
Semilobar holoprosencephaly is a subtype of holoprosencephaly characterized by incomplete forebrain division. It is intermediate in severity, being worse than lobar holoprosencephaly and better than alobar holoprosencephaly.
Epidemiology
Please refer to the general article of holoprosencephaly...
Article
Müllerian duct anomalies
Müllerian duct anomalies (MDAs) are congenital abnormalities that occur when the Müllerian ducts (paramesonephric ducts) do not develop correctly. This may be as a result of complete agenesis, defective vertical or lateral fusion, or resorption failure.
Epidemiology
MDAs are estimated to occur...
Article
Funneling of the internal cervical os
Cervical funnelling is a sign of cervical incompetence and represents the dilatation of the internal part of the cervical canal and reduction of the cervical length.
Greater than 50% funnelling before 25 weeks is associated with ~80% risk of preterm delivery.
Radiographic features
Good scanni...
Article
Inevitable miscarriage
Inevitable miscarriage refers to the presence of an open internal os in the presence of bleeding in the first trimester of pregnancy. Most often the conception products are not expelled and intracervical contents are present at the time of examination. A sac may be seen low within the uterus and...
Article
Ileal atresia
Ileal atresia is a congenital abnormality where there is significant stenosis or complete absence of a portion of the ileum. There is an increased incidence in those with chromosomal abnormalities.
This article will focus on ileal atresia alone but bear in mind that some cases correspond to jej...
Article
Myelomeningocele
Myelomeningocele, also known as spina bifida cystica, is a complex congenital spinal anomaly that results in spinal cord malformation (myelodysplasia).
Epidemiology
It is one of the commonest congenital CNS anomalies and thought to occur in approximately 1:500 of live births 5. There may be a...
Article
Chiari II malformation
Chiari II malformations are relatively common congenital malformations of the spine and posterior fossa characterized by myelomeningocele (lumbosacral spina bifida aperta) and a small posterior fossa with descent of the brainstem, cerebellar tonsils, and vermis through the foramen magnum. Numero...
Article
Ovarian hyperstimulation syndrome
Ovarian hyperstimulation syndrome (OHSS) is a complication of controlled ovarian stimulation, which is an assisted reproduction technique used for in vitro fertilisation (IVF). Rarely, it may also occur spontaneously in pregnancy (see below). It consists of ovarian enlargement with an extravascu...
Article
Congenital infections (mnemonic)
The group of the most common congenital infections are referred to by the mnemonic TORCH or STORCH. They usually cause mild maternal morbidity but are related to serious fetal consequences 4.
In cases where no serological, microbiological or immunological evidence of infection can be identified...
Article
Apgar score
Apgar score was originally described by Virginia Apgar (American anaesthesiologist, 1909-1974) in 1952.
Helpfully, her surname is also a useful mnemonic for remembering the 5 factors: each is graded as 0, 1 or 2 with a total possible score of 10. The lower the score the worse the prognosis.
Th...
Article
Ovarian artery
The ovarian artery is a paired structure and is the main gonadal artery in females.
Gross anatomy
Origin
The ovarian artery arises anterolaterally from the aorta just inferior to the renal arteries and superior to the inferior mesenteric artery (between L2 and L3).
Course
Descends caudally ...
Article
Uterine artery
The uterine artery is seen bilaterally and is a branch of the anterior division of the internal iliac artery.
Gross anatomy
Course
It runs medially in the pelvis, within the base of the broad ligament, to the outer surface of the uterus. From lateral to medial it has a descending, transverse ...
Article
Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease (ARPKD) is one of many pediatric cystic renal diseases.
On imaging, it usually presents on ultrasound with enlarged echogenic kidneys with multiple small cysts. Liver involvement with coarse echotexture, biliary tract cystic changes, and portal hype...
Article
Intrauterine contraceptive device
Intrauterine contraceptive devices (IUCD) (also known as intrauterine devices (IUD) and colloquially commonly as the coil) are one of the most frequently used methods of contraception throughout the world. It prevents pregnancy by:
thinning the endometrial lining
preventing sperm motility
pre...
Article
Fetal death in utero
Fetal death in utero (FDIU), also known as intrauterine death (IUD), is the term used when the death of a fetus occurs after the 20th week of pregnancy. Prior to this, it is considered a miscarriage.
Terminology
IUD is often also used as an abbreviation for an intrauterine contraceptive device...
Article
Vagina
The vagina is a midline fibromuscular tubular organ positioned in the female perineum extending superiorly from the vulva, to the cervix and uterus in the pelvis.
Gross anatomy
The vagina is 6-8 cm in length, extending posterosuperior from the vestibule through the urogenital diaphragm to the...
Article
Causes of oligohydramnios (mnemonic)
A helpful mnemonic for remembering some causes of oligohydramnios is:
DRIPPC
Mnemonic
D: demise
R: renal abnormalities (decreased urine output)
I: IUGR
P: premature rupture of membranes
P: post-dates
C: chromosomal anomalies
Article
Oligohydramnios
Oligohydramnios refers to a situation where the amniotic fluid volume is less than expected for gestational age. Often these fetuses have <500 mL of amniotic fluid. When there is almost no amniotic fluid present, this is termed anhydramnios.
Epidemiology
The estimated prevalence can be up to ~...
Article
Polyhydramnios
Polyhydramnios refers to a situation where the amniotic fluid volume is more than expected for gestational age.
It is generally defined as:
amniotic fluid index (AFI) >25 cm
largest fluid pocket depth (maximal vertical pocket (MVP)) greater than 8 cm 6
some centers, particularly in Australi...
Article
Twin-to-twin transfusion syndrome
Twin-to-twin transfusion syndrome (TTTS) is a potential complication that can occur in a monochorionic (either MCDA or MCMA) twin pregnancy.
Epidemiology
This complication can occur in ~10% (range 15-25%) of monochorionic pregnancies, giving an estimated prevalence of ~1:2000 of all pregnanci...
Article
Small for date fetus
A small for dates fetus can result from a number of factors
Fetal factors
aneuploidy
trisomy
triploidy
skeletal dysplasia(s)
structural anomalies (syndromes)
Maternal factors
Common
hypertension
medication(s):
fetal Warfarin syndrome
hydantoin embryopathy (Dilantin TM)
cytotoxic dru...
Article
Uterus
The uterus is an extraperitoneal hollow, thick-walled, muscular organ of the female reproductive tract that lies in the lesser pelvis.
Gross anatomy
The uterus has an inverted pear shape. It measures about 7.5 cm in length, 5 cm wide at its upper part, and nearly 2.5 cm in thickness in adults....
Article
Cervix
The cervix or uterine cervix is the lower constricted segment of the uterus providing the passage between the uterus proper and the vagina.
Gross anatomy
The cervix is somewhat conical in shape, with its truncated apex directed posteriorly and inferiorly. The inferior aspect of the cervix pro...
Article
Intracranial teratoma
Intracranial teratomas are uncommon intracranial neoplasms, which can have a bewildering variety of components and thus a wide range of appearances. They can be divided into two broad categories, intra- and extra-axial, which differ in epidemiology and clinical presentation. Another method of cl...
Article
Postpartum angiopathy
Postpartum angiopathy is a subset of reversible cerebral vasoconstriction syndrome (RCVS), although is has been described as a separate condition. It is also known as postpartum angiitis and puerperal vasospasm. Please refer to the main article on reversible cerebral vasoconstriction syndrome (R...
Article
Roberts syndrome
Roberts syndrome, also known as Roberts-SC phocomelia syndrome, pseudothalidomide syndrome, or Appelt-Gerken-Lenz syndrome, is a rare congenital malformation syndrome.
Clinical presentation
general
intrauterine growth restriction
postnatal growth retardation
failure to thrive
thrombocytope...
Article
Vein of Galen aneurysmal malformation
Vein of Galen aneurysmal malformations (VGAMs), probably better termed as median prosencephalic arteriovenous fistulas, are uncommon intracranial anomalies that tend to present dramatically during early childhood with features of a left-to-right shunt and high-output cardiac failure.
Epidemiolo...
Article
Uteroplacental blood flow assessment
Uteroplacental blood flow assessment is an important part of fetal well-being assessment and evaluates Doppler flow in the uterine arteries and rarely the ovarian arteries.
Pathology
In a non-gravid state and at the very start of pregnancy the flow in the uterine artery is of high pulsatility ...
Article
VACTERL association
VACTERL is an acronym that describes a non-random constellation of congenital anomalies. It is not a true syndrome as such and is equivalent to the VATER anomaly.
Epidemiology
The estimated incidence is 1 in 10,000-40,000 births 3.
Associations
Several conditions have features in common with...
Article
Twin peak sign
The twin peak sign, also known as the lambda (λ) sign, is the triangular appearance of the chorion insinuating between the layers of the intertwin membrane and strongly suggests a dichorionic diamniotic twin pregnancy. It is best seen in the first trimester (between 10-14 weeks) 5. While the pre...
Article
Turner syndrome
Turner syndrome, also known as 45XO or 45X, is the most common of the sex chromosome abnormalities in females.
Epidemiology
The incidence is estimated at 1:2000-5000 of live births, although the in utero rate is much higher (1-2% of conceptions) due to a significant proportion of fetuses with...
Article
Tubal ring sign
The tubal ring sign, also referred to as a bagel sign or blob sign, is one of the ultrasound signs of a tubal ectopic pregnancy. It comprises an echogenic ring that surrounds an unruptured ectopic pregnancy. It is said to have a 95% positive predictive value (PPV) for ectopic pregnancy.
Differe...
Article
Tubal ectopic pregnancy
Tubal ectopic pregnancy, also known as adnexal ectopic pregnancy, is the most common location of an ectopic pregnancy.
Epidemiology
It is the most common type of ectopic by far, accounting for 93-97% of cases.
Pathology
Although the fallopian tube has many anatomical parts, for the purposes ...
Article
Trisomies
The trisomies are chromosomal anomalies which usually occur due to non-disjunction. The vast majority of affected fetuses are spontaneously aborted, often very early during gestation. Only three are compatible with extrauterine life (T13, T18, T21), and only one beyond early infancy (T21).
In o...
Article
Threatened miscarriage
Threatened miscarriage (or threatened abortion) is mainly a clinical term, used when a pregnant woman in first 20 weeks of gestation presents with spotting, mild abdominal pain and contractions, with a closed cervical os 3.
Epidemiology
It occurs in 20-25% of pregnancies and is associated with...
Article
T sign (obstetrics)
The T sign is really the absence of a twin peak sign (or lambda (λ) sign) and is used in ultrasound assessment of a multifetal pregnancy.
It refers to the lack of chorion extending between the layers of the intertwin membrane, denoting a monochorionic pregnancy. The intertwin membrane comes to ...
Article
Strawberry skull
Strawberry skull refers to the shape of the head on an antenatal ultrasound.
Epidemiology
Associations
In general, strawberry skull is considered one of the non-specific 'soft markers' for abnormal fetal development. It is considered more closely associated with trisomy 18 (Edward syndrome).
...