TY - JOUR TI - Dyschromatosis universalis hereditaria: A rare case report from Northeast India AU - Bachaspatimayum, Romita AU - Das, Priyanka AU - Bhattacharjee, Nandita T2 - Our Dermatology Online AB - Dyschromatosis Universalis Hereditaria is a rare genodermatoses characterised by hyperpigmented and hypopigmented macules which are variable in size and shape. We report a case of Dyschromatosis Universalis Hereditaria from North east India who presented with multiple asymptomatic hyperpigmented and hypopigmented lesions over trunk and extremities since birth with positive family history which was later confirmed by histopathology. DA - 2019/04/09/ PY - 2019 DO - 10.7241/ourd.20192.18 DP - Zotero VL - 10 IS - 2 SP - 179 EP - 180 LA - en SN - 2081-9390 UR - http://www.odermatol.com/issue-in-html/2019-2-18-dyschromatosis/ ER -