Incontinentia pigmenti

Incontinentia pigmenti (IP) is a rare X-linked dominant multi-systemic ectodermal dysplasia usually lethal in males and presenting neonatally in females with a bullous rash along Blashko's lines (BL) followed by verrucous plaques evolving over time to hyperpigmented swirling patterns. It is further characterized by teeth abnormalities, alopecia, nail dystrophy and affects occasionally the retina and the central nervous system (CNS).

Cerebellar atrophy

Atrophy (wasting) of the cerebellum.


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PMID (PMCID)
8544960
MALE
Cerebellar involvement in hypomelanosis of Ito.
Pini G, Faulkner LB.
Neuropediatrics. 1995;26(4):208-10.
Hypomelanosis of Ito (HI) (incontinentia pigmenti achromians) with cerebellar atrophy and dysmorphic features is reported in a child.