Items tagged “congenital”

74 results found
Case

Scapular hypoplasia - dentate glenoid

 Diagnosis certain
Brian Gilcrease-Garcia
Published 10 Aug 2018
92% complete
X-rayCT
Case

Intestinal malrotation

 Diagnosis certain
Julius Rozmiarek
Published 07 Sep 2018
88% complete
FluoroscopyX-ray
Case

Anencephaly

 Diagnosis almost certain
Mostafa El-Feky
Published 24 Nov 2018
75% complete
Ultrasound
Case

Congenital hypertrophic pyloric stenosis

 Diagnosis certain
Mostafa El-Feky
Published 24 Nov 2018
91% complete
Ultrasound
Case

Cochlear aplasia

 Diagnosis certain
Jane McEniery
Published 29 Apr 2020
89% complete
MRI
Case

Congenital diaphragmatic hernia - Morgagni hernia

 Diagnosis probable
Hamza Shah
Published 17 Jul 2019
66% complete
X-ray
Article

Fossa of Waldeyer

The fossa of Waldeyer, also known as the mesentericoparietal fossa, is a congenital mesentery defect. It is found in about 1% of autopsy series and is formed due to non-fusion of the ascending mesocolon to the posterior parietal peritoneum. The superior mesenteric artery runs along its (anterio...
Article

Fossa of Landzert

The fossa of Landzert is a congenital mesentery defect. It is present in about 2% of autopsy series and is formed due to non-fusion of the inferior mesentery to the parietal peritoneum. It is found to the left of the fourth part of the duodenum. The inferior mesenteric vein runs along its (ante...
Case

Double outlet right ventricle with persistent left superior vena cava into coronary sinus (prenatal ultrasound)

 Diagnosis certain
Fabien Ho
Published 31 Dec 2019
94% complete
Ultrasound
Case

Klippel-Feil syndrome

 Diagnosis almost certain
Bassem Marghany
Published 17 Mar 2020
72% complete
X-ray
Case

Left occipital petalia

 Diagnosis certain
Mohd Radhwan Bin Abidin
Published 09 Jul 2020
89% complete
MRI
Article

Megalocornea

Megalocornea is a rare bilateral congenital ocular defect characterized by a corneal diameter of more than 13 mm with the deep anterior chamber and normal intraocular pressure 1-3. Epidemiology Megalcornea is associated with Chordin-like 1 (CHRDL1) gene mutation 1,2. It is associated with mult...
Case

Band heterotopia

 Diagnosis almost certain
Sovann Vathana Lay
Published 22 Sep 2021
77% complete
MRI
Case

Aphakia

 Diagnosis certain
Ashesh Ishwarlal Ranchod
Published 14 Mar 2022
98% complete
CT