క్లినికల్ పీడియాట్రిక్ డెర్మటాలజీ అందరికి ప్రవేశం

నైరూప్య

Dyschromatosis in a Child - A Case Report and Differential Diagnosis

Doss RW

Dyschromatoses are rare group of disorders characterized by the presence of both hyperpigmented and hypopigmented macules, many of which are small in size and irregular in shape. The dyschromatoses spectrum includes dyschromatosis universalis hereditaria, dyschromatosis symmetrica hereditaria, acropigmentation of Dohi, and a segmental form called unilateral dermatomal pigmentary dermatosis. We report a case of dyschromatosis in an 8-year old girl. The patient presented with a history of ephelids in face that appeared during the first year of life, Hyperpigmented and hypopigmented lesions that were noticed at cheeks, forehead, chin, back and extremities. This is the first case of dyschromatosis universalis reported to be associated light colored hair, eyebrows and eye lashed and hyperhidrosis.

నిరాకరణ: ఈ సారాంశం ఆర్టిఫిషియల్ ఇంటెలిజెన్స్ టూల్స్ ఉపయోగించి అనువదించబడింది మరియు ఇంకా సమీక్షించబడలేదు లేదా నిర్ధారించబడలేదు
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