205 results found
Case
Dyke-Davidoff-Mason syndrome
Published
09 Feb 2016
90% complete
MRI
Article
Dyke-Davidoff-Masson syndrome
Dyke-Davidoff-Masson syndrome is a condition characterized by hemicerebral atrophy/hypoplasia secondary to brain insult usually in fetal or early childhood period and is accompanied by ipsilateral compensatory osseous hypertrophy and contralateral hemiparesis.
It is characterized by:
thickenin...
Case
Dyke-Davidoff-Masson syndrome
Published
23 Jun 2013
77% complete
MRI
Case
Dyke-Davidoff-Masson syndrome
Published
24 Jan 2021
77% complete
MRI
Case
Dyke-Davidoff-Masson syndrome
Published
25 Jan 2024
71% complete
CT
Case
Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy
Published
25 Jan 2022
68% complete
MRI
Case
Elderly CT brain
Published
24 Nov 2014
56% complete
CT
Article
Encephalocraniocutaneous lipomatosis
Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland syndrome, is a rare congenital neurocutaneous syndrome characterized by unilateral lipomas of the cranium, face, and neck, ipsilateral lipodermoids of the eye, and ipsilateral brain anomalies.
The clinical features of ECCL ove...
Case
Evolution of cerebral infarction: edema to laminar necrosis and hemorrhagic transformation then to atrophy
Published
23 Dec 2014
95% complete
CT
Playlist
Evolution of cerebral infarction: oedema to laminar necrosis and haemorrhagic transformation then to atrophy
1 case
No description provided
Playlist
Evolution of cerebral infarction: oedema to laminar necrosis and haemorrhagic transformation then to atrophy
1 case
No description provided
Case
Fahr disease
Published
12 Dec 2013
71% complete
CT
Case
Fahr disease
Published
21 Aug 2010
39% complete
CT
Case
Fahr disease
Published
27 Apr 2015
62% complete
CT
Article
Fahr syndrome
Fahr syndrome, also known as bilateral striatopallidodentate calcinosis, is characterized by abnormal vascular calcium deposition, particularly in the basal ganglia, cerebellar dentate nuclei, and white matter, with subsequent atrophy.
It can be either primary (usually autosomal dominant) or se...
Case
Fragile X-associated tremor/ataxia syndrome
Published
13 Jun 2016
94% complete
CT
MRI
Article
Fragile X-associated tremor/ataxia syndrome
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive degenerative movement disorder resulting from a fragile X “premutation”, defined as 55-200 CGG repeats in the 5’-untranslated region of the FMR1 gene 1. The premutation can expand in subsequent generations (during oogenesis) to...
Article
Friedreich ataxia
Friedreich ataxia is the most common hereditary progressive ataxia.
Epidemiology
Thought to have an estimated prevalence of ~1:50,000. There is no recognized gender predilection.
Typically present in childhood to adolescence 11. Those with a higher number of trinucleotide repeats (>500) are t...
Article
Frontal lobe
The frontal lobe is by far the largest of the four lobes of the cerebrum (other lobes: parietal lobe, temporal lobe, and occipital lobe), and is responsible for many of the functions which produce voluntary and purposeful action.
Gross anatomy
The frontal lobe is the largest lobe accounting fo...
Case
Frontotemporal lobar degeneration with caudate atrophy
Published
01 Nov 2012
62% complete
Annotated image
CT
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