Dermatoleukodystrophy

Orpha code: 1659OMIM code: 221790

Definicja

A rare leukodystrophy characterized by congenital thickened, wrinkled skin showing loss of elasticity, in combination with childhood onset of rapidly progressive generalized cognitive and motor impairment quickly resulting in a vegetative state and early death. Neuropathologic examination reveals neuroaxonal leukodystrophy with numerous neuroaxonal spheroids and diffuse loss of axons and myelin sheaths.

Disease data
Klasyfikacja

Disease

Synonimy
Cutis laxa-leukodystrophy
Kod ORPHA
1659
Kod OMIM
221790
Kod ICD10
E75.2
Kod ICD11
-

No additional description.

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