Dyschromatosis Symmetrica Hereditaria of Late Onset?

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Dyschromatosis Symmetrica Hereditaria of Late Onset?

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 with reticulated pattern. This paper presents a female patient with typical dermatological lesions, but only diagnosed in adulthood. It is necess...

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Dyschromatosis symmetrica hereditaria: a pedigree study

Dyschromatosis symmetrica hereditaria (DSH), also known as reticulate acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypoand hyper-pigmented macules in varying sizes on the dorsal extremities with reticulated pattern. This paper presents an unmarried Chinese male patient with typical dermatological lesions. Four generations of the family with 2...

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Dyschromatosis Symmetrica Hereditaria and RNA Editing Enzyme

Dyschromatosis symmetrica hereditaria (DSH) is a highly penetrant autosomal-dominant skin disease. It is characterized by a mixture of hyperand hypo-pigmented macules on the dorsal aspects of the hands and feet (Figure 1). The disorder typically has its onset during infancy or early childhood, stops spreading before adolescence and lasts for life. It was clarified in 2003 that a heterozygous mu...

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Dyschromatosis symmetrica hereditaria with cutaneous lupus erythematosus and hyperthyroidism

Dyschromatosis symmetrica hereditaria (DSH) is a rare genodermatosis characterized by various sizes of both hyper- and hypopigmented macules arranged in reticulated patterns on the face and the dorsal aspects of the extremities. There are also cutaneous and extracutaneous abnormalities, but they are rare. As far as we know, DSH associated with immune-mediated conditions has not been reported. W...

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Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review

Background/Objective: Dyschromatosis symmetrica hereditaria (DSH) is a rare pigmentary genodermatosis characterized by hyperand hypopigmented macules on the face and dorsal aspects of the extremities. This study aimed to delineate the unique clinical, histological, and genetic features of DSH in a Taiwanese population. Methods: A retrospective review of clinical charts and archival photographs ...

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ژورنال

عنوان ژورنال: Case Reports in Dermatological Medicine

سال: 2014

ISSN: 2090-6463,2090-6471

DOI: 10.1155/2014/639537