Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome

Orpha code: 496641OMIM code: 617193

Definition

A rare, severe early-onset neurodegenerative encephalopathy characterized mainly by developmental delay (DD) / developmental regression (DR), epilepsy, cortical atrophy, secondary hypomyelination and thin corpus callosum. Additional features include secondary microcephaly, hypotonia, spasticity, optic atrophy and skeletal anomalies.

Disease data
Classification

Malformation syndrome

ORPHA code
496641
OMIM code
617193
ICD10 code
-
ICD11 code
-

No additional description.

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