180 results found
Case
Intracranial hypotension: iatrogenic
Published
14 Feb 2016
100% complete
MRI
CT
Case
Cerebral vasculitis
Published
02 Apr 2017
74% complete
MRI
Article
Wolfram syndrome (type one)
Wolfram syndrome type one, also known as DIDMOAD, is a disease caused by an autosomal recessive genetic trait, caused by mutations in the WFS1 gene, with incomplete penetrance.
Clinical presentation
The syndrome presents initially with type 1 diabetes mellitus, followed by optic atrophy, diabe...
Case
Glioblastoma IDH wild-type (radiation induced)
Published
18 Mar 2015
95% complete
MRI
Pathology
Case
Subdural hemorrhage
Published
06 Nov 2020
95% complete
CT
Case
Artery of Percheron territory old infarction
Published
03 Feb 2024
95% complete
MRI
Case
Subdural hygroma
Published
27 Dec 2012
92% complete
MRI
Case
Solvent abuse
Published
02 Apr 2012
92% complete
MRI
Article
Niemann-Pick disease type C
Niemann-Pick disease type c (NPD-C or just NPC) is an autosomal recessive lysosomal storage disorder classed under Niemann-Pick disease on account of clinical similarities, namely hepatosplenomegaly and variable involvement of the central nervous system.
Epidemiology
NPD-C is inherited as an ...
Case
Viral encephalitis- sequelae
Published
11 Apr 2021
81% complete
MRI
CT
Case
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Published
06 Mar 2022
81% complete
CT
MRI
Case
Brain metastases from lung cancer associated with metastasis to the pineal gland
Published
08 Oct 2023
80% complete
Annotated image
CT
Article
Ataxia-telangiectasia
Ataxia-telangiectasia, also known as Louis-Bar syndrome, is a rare multisystem autosomal recessive disorder, sometimes classified as a phakomatosis. It is characterized by multiple telangiectasias, cerebellar ataxia, pulmonary infections, and immunodeficiency.
On brain imaging, it usually demo...
Case
Mucopolysaccharidosis type VI
Published
04 Dec 2020
77% complete
MRI
Case
Hyperdense thalami-perinatal ischemia
Published
06 Nov 2020
77% complete
CT
Case
Medial temporal lobe atrophy
Published
10 Jul 2015
77% complete
MRI
Annotated image
Case
Neuronal ceroid lipofuscinosis
Published
05 Dec 2021
77% complete
MRI
Article
Tuberous sclerosis
Tuberous sclerosis (TS), also known as tuberous sclerosis complex (TSC) or Bourneville disease, is a phakomatosis (neurocutaneous disorder) characterized by the development of multiple benign tumors of the embryonic ectoderm (e.g. skin, eyes, and nervous system).
Epidemiology
Tuberous sclerosi...
Article
Cockayne syndrome
Cockayne syndrome is a rare autosomal recessive dysmyelinating disease. Cockayne syndrome is classified among the childhood leukodystrophies, and brain imaging findings are cardinal features suggesting the diagnosis of Cockayne syndrome. Previously published Cockayne syndrome imaging studies hav...
Case
Cerebral fat embolism (type 2A) - confluent edema in white matter
Published
09 Mar 2022
68% complete
X-ray
CT
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