Linear and whorled nevoid hypermelanosis

Orpha code: 79150OMIM code: 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.

Disease data
Klasyfikacja

Disease

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

No additional description.

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