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Incontinentia pigmenti

MONDO:0010631

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).

Also known as: Bloch-Siemens syndrome, Bloch-Sulzberger syndrome, Incontinentia pigmenti syndrome, incontinentia pigmenti, incontinentia pigmenti, X-linked dominant, IP, IP2 (formerly), Incontinentia pigmenti type 2 (formerly)

31 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Retinal disorder (79) Syndromic disease (24) Human disease (14) Hereditary neurological disease (5) Hereditary skin disorder (5)
Trials to join now! 21 Not yet recruiting 2 Not yet finished but already full! 3 Completed 4 Terminated 1
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