Results 41 to 50 of about 401 (136)

Dyschromatosis universalis hereditaria in three siblings

Pigment International, 2016
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis, which has been reported most often from Japan. The etiology of this disorder is not yet known. DUH is characterized by mixtures of hyperpigmented- and hypopigmented macules all over the body. Skin lesions are usually present in the first years of life.
YJ Bhat, I Latief, I Hassan
openaire   +2 more sources

Generalized reticulated hyperpigmented patches interspersed with hypopigmented macules [PDF]

JAAD Case Reports, 2021
Meshal Mohammad Alhameedy, MD
doaj   +2 more sources

Preventing transmission of dyschromatosis universalis hereditaria through preimplantation genetic testing: A case report. [PDF]

World J Clin Cases
Wang XL, Zou T, Wu YC, Weng YY, Yao Q, Sun WW.   +5 more
europepmc   +2 more sources

Inherited Reticulate Pigmentary Disorders. [PDF]

Genes (Basel), 2023
Reticulate pigmentary disorders (RPDs) are a group of inherited and acquired skin conditions characterized by hyperpigmented and/or hypopigmented macules.
Lin MH, Chou PC, Lee IC, Yang SF, Yu HS, Yu S.   +5 more
europepmc   +2 more sources

Dyschromatosis universalis hereditaria with <i>SASH1</i> mutation improved with picosecond laser treatment. [PDF]

Skin Health Dis
Yuan L, Luo Y, Yang C, Man MQ, Yang B, Liu Z.   +5 more
europepmc   +3 more sources

Dyschromatosis Universalis Hereditaria

Kathmandu University Medical Journal, 2021
Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary genodermatosis usually inherited in autosomal dominant fashion characterized by multiple pinpoint to pea-sized hypo- and hyper-pigmented macules arranged in reticulate pattern that develops within the first few years of life.
M, Bista, S, Agrawal, Y, Agrawal
openaire   +2 more sources

De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper‐ and Hypo‐pigmentation (FPHH)

Molecular Genetics &Genomic Medicine, Volume 9, Issue 12, December 2021., 2021
Abstract Familial Progressive Hyper‐ and Hypopigmentation is a pigmentary disorder characterized by a mix of hypo‐ and hyperpigmented lesions, café‐au‐lait spots and hypopigmented ash‐leaf macules. The disorder was previously linked to KITLG and various mutations have been reported to segregate in different families.
Mario Gorenjak, Nino Fijačko, Pij Bogomir Marko, Milanka Živanović, Uroš Potočnik   +4 more
wiley   +1 more source

Acral persistent papular mucinosis with lichenoid drug reaction due to isotretinoin on background of dyschromatosis universalis hereditaria

Clinical Dermatology Review, 2023
T Ramprasanth, Yugal K Sharma, Mahendra Singh Deora, Aayush Gupta   +3 more
doaj   +2 more sources

Acropigmentation of DohiA Rare Presentation [PDF]

Journal of Clinical and Diagnostic Research, 2021
Reticulate Acropigmentation of Dohi or Dyschromatosis symmetrica hereditaria, is an autosomal dominant genodermatosis, with very few reported autosomal recessive traits mostly seen in the Japanese population.
SAMIKSHA DEEPAK CHAVHAN, SUGAT JAWADE, BHUSHAN MADKE, ADARSHLATA SINGH   +3 more
doaj   +1 more source

Dyschromatosis Universalis Hereditaria [PDF]

Annals of Dermatology, 1990
Young Suck Ro, Tchae Sik Nam, Chang Woo Lee, Chan Kum Park, Weoun Pheel Seou, Jae Hong Kim   +5 more
openaire   +2 more sources