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Ferro-cerebro-cutaneous syndrome

ORPHA:397922· ICD-10 G31.8

Definition

A rare neurodegenerative disease characterized by progressive neurodegeneration, cutaneous abnormalities, including varying degrees of ichthyosis or seborrheic dermatitis, and systemic iron overload. Patients manifest with infantile-onset seizures, encephalopathy, abnormal eye movements, axial hypotonia with peripheral hypertonia, brisk reflexes, cortical blindness and deafness, myoclonus and hepato/splenomegaly, as well as oral manifestations, including microdontia, widely spaced and pointed teeth with delayed eruption, and gingival overgrowth.

Prevalence
<1 / 1 000 000
Inheritance
X-linked recessive
Age of onset
Infancy