Dziedziczna poikilodermia z akrokeratozą

Kod Orpha: 2907Kod OMIM:

Definicja

A rare hereditary poikiloderma characterized by infantile onset of vesicopustule formation on hands and feet and widespread eczematoid dermatitis (both spontaneously resolving during childhood), as well as gradually developing diffuse poikiloderma with striate and reticulate atrophy (excluding the face, scalp, and ears), and development of keratotic papules on hands, feet, elbows, and knees, beginning in early childhood. There have been no further descriptions in the literature since 1981.

Dane
Klasyfikacja

Choroba

Synonimy
Weary syndrome
Wrodzona poikilodermia z pęcherzami, typu Weary
Kod ORPHA
2907
Kod OMIM
-
Kod ICD10
Q82.8
Kod ICD11
LD2B

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