Description of the disease * EnglishPolish Pobierz sekcję do PDF 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. Disease data Klasyfikacja Disease Synonimy Weary syndrome Wrodzona poikilodermia z pęcherzami, typu Weary Kod ORPHA 2907 Kod OMIM - Kod ICD10 Q82.8 Kod ICD11 LD2B *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl