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).

Impaired neutrophil chemotaxis

An impairment of the migration of neutrophils towards chemoattractants as part of the innate immune response


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PMID (PMCID)
8726652
FEMALE Adult
Incontinentia pigmenti and Behcet's disease: a case of impaired neutrophil chemotaxis.
Endoh M, Yokozeki H, Maruyama R, Matsunaga T, Katayama I, Nishioka K.
Dermatology. 1996;192(3):285-7.
Incontinentia pigmenti and Behcet's disease: a case of impaired neutrophil chemotaxis.