Linear and whorled nevoid hypermelanosis

Kod Orpha: 79150Kod OMIM: 614323

Definicja

A rare hyperpigmentation of the skin disease characterized by the congenital to infantile-onset of bilateral, diffuse (occasionally localized), reticulate (swirls and streaks), macular hyperpigmentation following the lines of Blaschko, typically involving the trunk, limbs, head and neck (but sparing palms, soles and mucosa), without preceding inflammation, blistering or atrophy. Occasionally, extracutaneous abnormalities, including autism, seizures, cardiac defects, skeletal abnormalities and developmental delay, may be associated. Histologically, basal and/or suprabasal melanosis, without pigment incontinence, is observed.

Dane
Klasyfikacja

Choroba

Synonimy
LWNH
LWNH
Kod ORPHA
79150
Kod OMIM
614323
Kod ICD10
L81.4
Kod ICD11
EC23.0

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