Results 111 to 120 of about 401 (136)

Investigating the Prevalence, Gender Predilection, and Inheritance Patterns of Genodermatoses: A Tertiary Hospital Study. [PDF]

Cureus
Puttur N, Kapoor A, Lakhey K, Reddy A, Malik N, Deokar S.   +5 more
europepmc   +1 more source

Amyloidosis Cutis Dyschromica: A Rare Subtype of Primary Cutaneous Amyloidosis with Dermoscopy.

Indian J Dermatol
Priyadhashini BV, Agrawal I, Sahoo B, Mandal S.   +3 more
europepmc   +1 more source

Dermoscopy of Familial Gigantic Melanocytosis: A Report of Rare Entity.

Indian J Dermatol
Ankad BS, Nikam BP, Chigurupati E.
europepmc   +1 more source

A Case of Dyschromatosis Universalis Hereditaria-Simultaneous Occurrence of Amyloid Deposition

, 1983
Naohide Takehara, Hidetoshi Nakayama, Rumi Makino, Motoyuki Mihaka, Shuhei SHIMAO, S. Shimao, Isao Matsumoto   +6 more
openalex   +1 more source

Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria [PDF]

Experimental Dermatology, 2023
AbstractDyschromatosis universalis hereditaria (DUH) is characterized by diffuse symmetrically distributed hypopigmented macules mixed with hyperpigmentation. DUH is divided into three types by Online Mendelian inheritance in man (OMIM) that is, DUH1 (OMIM 127500), DUH2 (OMIM 612715) and DUH3 (OMIM 615402) according to the different linkage regions ...
Ding'An Zhou
exaly   +4 more sources

Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature

Pediatric Dermatology, 2002
Abstract: We describe dyschromatosis universalis in a 19‐month‐old Saudi Arabian girl. She had no associated defects and none of the other family members were affected. Similar cases reported from countries other than the Far East, where the disease was first described, are discussed.
Khalid Al Aboud, Daifullah Al Aboud
exaly   +4 more sources

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Dyschromatosis universalis hereditaria

International Journal of Dermatology, 2023
AbstractReticulate pigmentary dyschromatoses primarily include dyschromatosis universalis hereditaria (DUH), dyschromatosis symmetrica hereditaria (DSH) (Reticulate acropigmentation of Dohi), and unilateral dermatomal pigmentary dermatosis, which differ in their patterns of distribution.
Aravind Baskar Murthy, Kaliaperumal Karthikeyan   +1 more
exaly   +3 more sources

Dyschromatosis universalis hereditaria

Clinical and Experimental Dermatology, 2002
Dyschromatosis universalis hereditaria is a clinically heterogenous disorder. We report two unrelated Indian patients with dyschromatosis universalis hereditaria, who had generalized and progressive reticulate hyper- and hypo-pigmentation of the skin. The oral mucosa and tongue also showed mottled pigmentation.
Gomathy Sethuraman, M D'Souza, Devinder Mohan Thappa   +2 more
exaly   +3 more sources

Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation

American Journal of Medical Genetics Part A, 2003
AbstractWe report a familial case of dyschromatosis universalis hereditaria (DUH) which is compatible with an autosomal dominant inheritance. The male proband from Bangladesh presented with randomly distributed hyper‐ and hypo‐pigmented skin lesions of variable shape and size with a mottled appearance.
Nuber, U., Tinschert, S., Mundlos, S., Hauber, I.   +3 more
core   +9 more sources

Dyschromatosis Universalis Hereditaria: An Electron Microscopic Examination

Journal of Dermatology, 1997
AbstractWe report electron microscopic findings from both hyperchromic and achromic macules of dyschromatosis universalis hereditaria (DUH). The keratinocytes of the hyperchromic macules contained numerous, fully melanized melanosomes; almost all of them were aggregated to form the melanosome complex.
Sungbin Im, Soo-Chan Kim, N S Kim
exaly   +3 more sources