Results 11 to 20 of about 695 (177)
Dyschromatosis Symmetrica Hereditaria of Late Onset? [PDF]
Case Reports in Dermatological Medicine, 2014 Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo- and hyperpigmented macules of varying sizes on the dorsal of the extremities ...
Caroline Balvedi Gaiewski +3 more
doaj +4 more sources
Dyschromatosis symmetrica hereditaria
Journal of Clinical and Scientific ResearchDyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterised by a mixture of hyperpigmented and hypopigmented macules on the dorsal aspects of the hands and feet.
K. Geetha
doaj +3 more sources
Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders [PDF]
Dermatology Research and Practice, 2017 Reticulated pigmentation is a unique pigmentary change caused by a heterogeneous group of hereditary and acquired disorders. This pigmentation is characterized by a mottled appearance, with lesions that vary in size and pigmentary content.
H. Alshaikh, F. Alsaif, S. Aldukhi
doaj +3 more sources
Dyschromatosis symmetrica hereditaria with cutaneous lupus erythematosus and hyperthyroidism
International Medical Case Reports Journal, 2017 Fahad Al-Saif,1 Ahmed Alhumidi,2 Rama Ayed Alhallaf1 1Dermatology Department, 2Pathology Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia Abstract: Dyschromatosis symmetrica hereditaria (DSH) is a rare genodermatosis ...
Ahmed Alhumidi
exaly +3 more sources
Two Novel and Two Recurrent Variants of the ADAR1 Gene in Three Chinese Families with Dyschromatosis Symmetrica Hereditaria [PDF]
Clinical, Cosmetic and Investigational DermatologyYunxia Zhu,1 Deng Zhang,1 Liang Wu,1 Xiaoliang Ouyang,2 Shengcai Zhu,1 Xiuping Wang,1 Zhen Xiao,3 Yanping Tan,4 Chunming Li1 1Department of Dermatology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi ...
Zhu Y +8 more
doaj +4 more sources
Dyschromatosis universalis hereditaria: A rare case report
Journal of Mahatma Gandhi Institute of Medical Sciences, 2013 Dyschromatosis universalis hereditaria is an autosomal dominant disorder but may be recessive or sporadically inherited disorder, infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled ...
Esha Bisne, Sonia Jain, V B Shivkumar
doaj +2 more sources
Dyschromias: A series of five interesting cases from India
Indian Journal of Dermatology, 2015 Dyschromatosis is a pigmentary genodermatosis which presents with hyper and hypopigmented skin lesions giving a mottled appearance. It is a rare entity in India reported mainly in the East Asian population.
Prabhu Namitha, S Sacchidanand
doaj +2 more sources
Sporadic dyschromatosis universalis hereditaria: A rare case report
Indian Journal of Paediatric Dermatology, 2017 Dyschromatosis universalis hereditaria (DUH) is a rare genodermatoses characterized by hyperpigmented and hypopigmented macules inherited most commonly in autosomal dominant manner.
Shweta Manchanda +2 more
doaj +2 more sources
Indian Journal of Dermatology, 2012 Reticulate acropigmentation of Dohi also called dyschromatosis symmetrica hereditaria or symmetrical dyschromatosis of the extremities is an autosomal dominant inherited disorder.
Deepak Mohana +3 more
doaj +2 more sources
A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
Indian Dermatology Online Journal, 2015 Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Sumir Kumar +2 more
doaj +2 more sources