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

Orpha code: 496641OMIM code: 617193

Definicja

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
Klasyfikacja

Malformation syndrome

Kod ORPHA
496641
Kod OMIM
617193
Kod ICD10
-
Kod ICD11
-

No additional description.

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