Results 81 to 90 of about 695 (177)
Dowling-Degos Disease: Case Report and Review of the Literature [PDF]
, 2010 Dowling-Degos disease (DDD) is an unusual pigmentary disorder usually caused by mutations in keratin 5. A 44-year-old woman in good general health presented due to the recent appearance of numerous pigmented macules on her axillary and anogenital skin. A
Batycka-Baran, Aleksandra +3 more
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Acquired brachial cutaneous dyschromatosis in a middle aged male
, 2018 Acquired brachial cutaneous dyschromatosis (ABCD) is an acquired disorder of pigmentary change that presents as chronic, asymptomatic, geographic-shaped, gray-brown patches, consisting of mixed hyper and hypopigmented macules on the dorsal aspect of the ...
최유원, 최혜영, 변지연
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Dyschromatosis Universalis Hereditaria with bilateral keratopathy – A case report
Indian Journal of Ophthalmology. Case ReportsA 14-year-old male presented with bilateral corneal thinning and opacification. Clinical examination revealed impending perforation of the right eye. There was a history of pigmented macules all over the trunk and extremities, as well as buccal mucosa ...
Neha Kumari +3 more
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Caso para diagnóstico Case for diagnosis
Anais Brasileiros de Dermatologia, 2009 A discromatose simétrica hereditária (acropigmentação de Dohi) é alteração pigmentar rara, genética, com padrão de herança autossômica dominante. Caracteriza-se por máculas hiper e hipocrômicas com padrão mosqueado e distribuição acral.
Giselle Carvalho Froes +2 more
doaj +1 more source
Acquired Brachial Cutaneous Dyschromatosis: A Rarely Recognized Condition
Dermatology Practical & Conceptual, 2021 Jorge Román-Sainz +3 more
doaj +1 more source
Folia Neuropathologica, 2016 Pathogenic molecular variants in the ADAR gene are a known cause of rare diseases, autosomal recessive Aicardi- Goutières syndrome type 6, severe infantile encephalopathy with intracranial calcifications and dominant dyschromatosis symmetrica hereditaria,
Dorota Piekutowska-Abramczuk +9 more
doaj +1 more source
Erythema dyschromicum perstans following neurotoxin injection for facial rhytides
JAAD Case Reports, 2023 Corley C. Pruneda, MD +3 more
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Atypical cases of Dowling-Degos disease
Indian Dermatology Online Journal, 2016 Dowling–Degos disease (DDD) is a rare autosomal dominant condition characterized by multiple, small, round pigmented macules usually arranged in reticular pattern, chiefly distributed in axillae and groins.
Kikkeri Narayanshetty Naveen +5 more
doaj +1 more source
Dyschromatosis universalis hereditaria: A case report
Dermatology Online Journal, 2011 Dyschromatosis universalis hereditaria (DUH) is usually an autosomal dominantly inherited disorder characterized by the presence of hypopigmented as well as hyperpigmented macules. We report an Indian patient with DUH with widespread involvement of skin including the face, oral mucous membranes (including tongue), and palms and soles.
Udayashankar, Carounanidy +1 more
openaire +4 more sources
, 2003 Dyschromatosis symmetrica hereditaria (DSH) is a hereditary skin disease characterized by the presence of hyperpigmented and hypopigmented macules on extremities and face.
Feng, Guo-yin +10 more
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