Items tagged “cases”

5,524 results found
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Neurocandidiasis

Neurocandidiasis results from disseminated infection of the central nervous system by the fungus Candida albicans, usually manifesting as cerebral microabscesses and meningitis. Epidemiology CNS disease is thought to occur in up to 52% of patients with disseminated candidiasis, but predominate...
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Variably protease-sensitive prionopathy

Variably protease-sensitive prionopathy (VPSPr) is a very rare type of sporadic human prion disease that was first described in 2008. Epidemiology Variably protease-sensitive prionopathy is very rare, with an annual incidence of 1-2 per million 5. Clinical presentation Clinical presentation ...
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Endophthalmitis

Endophthalmitis (plural: endophthalmitides) is a potentially sight-threatening condition that involves intraocular inflammation of any cause. It is distinguished from panophthalmitis in that it does not extend beyond the sclera. It is either infectious or non-infectious in etiology, but in clini...
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Hematomyelia

Hematomyelia refers to the presence of intramedullary hemorrhage or hematoma within the spinal cord. This is distinct from extramedullary hemorrhage such as that seen in epidural hematoma. Pathology Although hematomyelia can occur in the setting of trauma, the term is generally used to signify...
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Eastern equine encephalitis

Eastern equine encephalitis (EEE) is one of many viral encephalitides and results from infection with the eastern equine encephalitis virus. Clinical presentation Most patients have non-specific viral prodromal symptoms for approximately one week, including fevers, headache, nausea and vomitin...
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Murray Valley encephalitis

Murray Valley encephalitis (MVE), also known as Australian encephalitis, is one of many viral encephalitides and Flavivirus encephalitides, resulting from infection with the Murray Valley encephalitis virus. Clinical presentation Most patients have non-specific viral prodromal symptoms for app...
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Non-ketotic hyperglycemic seizure

Non-ketotic hyperglycemic seizures are one of the neurological complications of non-ketotic hyperglycemia, along with non-ketotic hyperosmolar coma and non-ketotic hyperglycemic hemichorea.  Epidemiology Seizures in the context of non-ketotic hyperglycemia are most frequently reported in middl...
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Aceruloplasminemia

Aceruloplasminemia is an autosomal recessive type of neurodegeneration with brain iron accumulation and disorder of iron metabolism caused by a mutation in the ceruloplasmin (CP) gene resulting in the production of dysfunctional ceruloplasmin. Epidemiology Aceruloplasminemia is a very rare dis...
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11-13 week antenatal scan

11-13 week antenatal (nuchal translucency) scan is considered a routine investigation advised for fetal well-being as well as for early screening in pregnancy (see antenatal screening). It includes multiple components and is highly dependent on the operator. Traditionally three factors are used...
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Coronary arteriovenous fistula

Coronary arteriovenous fistulas (CAVFs) are rare coronary artery anomalies whereby there is a fistula between a coronary artery and, most commonly, the right side of the cardiac circulation.  Terminology Although a CAVF, in the strictest sense of the term, implies a communication between the c...
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Langerhans cell histiocytosis (CNS manifestations)

The central nervous system (CNS) is an uncommonly involved organ system in Langerhans cell histiocytosis (LCH). Involvement of the CNS is related but distinct from involvement of the skull or craniofacial structures, which are discussed separately in the article skeletal manifestations of LCH. F...
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Cochlear incomplete partition type II

Cochlear incomplete partition type II (IP-II) is a type of inner ear malformation, specifically a cochlear incomplete partition, associated with sensorineural hearing loss. It is characterized by a cystic cochlear apex and should not be confused with Mondini anomaly, which is a historic term for...
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Small lung volume (differential diagnosis)

The following differential diagnoses can be considered when small lung volumes are seen: pulmonary fibrosis prior surgery, e.g. lobectomy, lung volume reduction surgery pleural disease, e.g. pleural thickening skeletal deformities, e.g. kyphosis, scoliosis systemic lupus erythematosus (SLE)...
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Dorsal columns

The dorsal columns, or posterior columns, are ascending pathways primarily concerned with sensory function. They are responsible for transmitting vibration, conscious proprioception, and fine (discriminative) touch 1,2. The dorsal columns are divided two tracts, which are discussed separately 2...
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Gracile fasciculus

The gracile fasciculus, also known as the fasciculus gracilis (plural: fasciculi graciles) or column of Goll, represents the medial portion of the dorsal columns and carries input from below and including T7 1. Function The gracile fasciculus is responsible for transmitting vibration, consciou...
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Fusiform intracranial aneurysm

Fusiform intracranial aneurysms are a type of intracranial aneurysms with an elongated fusiform shape caused by atherosclerotic disease most common in the vertebrobasilar circulation. Epidemiology 3%-13% of all intracranial aneurysms Clinical presentation They can be incidental or asymptomat...
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RASopathy

RASopathies are a class of developmental disorders caused by germline mutations in genes that encode for components or regulators of the Ras/mitogen-activated protein kinase (MAPK) pathway. Epidemiology As a group, RASopathies represent one of the most common malformation syndromes, with an in...
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Hemifacial hypertrophy

Hemifacial hyperplasia or hemifacial hypertrophy is a rare developmental anomaly characterized by asymmetric growth of hard and soft tissues of the face 1. Epidemiology These asymmetries are often noted at birth and are usually accentuated with increasing age, especially around puberty 2. The...
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Enterovirus rhombencephalitis

Enterovirus rhombencephalitis is the most common neurological complication of enterovirus infection 1. Clinical presentation Enterovirus rhombencephalitis causes acute and severe neurologic disorders such as ataxia, nystagmus, oculomotor palsies, or bulbar palsy. In some cases, neurologic affe...
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Arachnoiditis ossificans

Arachnoiditis ossificans is considered a sequela of chronic arachnoiditis where there is a development of calcification-ossification of the arachnoid membrane usually of the thoracic and lumbar spines. It is an extremely rare cause of spinal canal stenosis and consequent neurological compromise....

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