| Dyschromatosis universalis hereditaria: A rare entity. | |
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MedLine Citation:
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PMID: 21810391 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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Dyschromatosis universalis hereditaria is an infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled hyperpigmented and hypopigmented macules that give an overall impression of mottling. We hereby report a case of dyschromatosis universalis hereditaria in a young female with a family history of the disorder. |
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Authors:
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Sumir Kumar; Bharat Bhushan Mahajan; Rajwinder Singh |
Publication Detail:
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Type: Journal Article Date: 2011-07-15 |
Journal Detail:
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Title: Dermatology online journal Volume: 17 ISSN: 1087-2108 ISO Abbreviation: Dermatol. Online J. Publication Date: 2011 |
Date Detail:
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Created Date: 2011-08-03 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9610776 Medline TA: Dermatol Online J Country: United States |
Other Details:
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Languages: eng Pagination: 6 Citation Subset: IM |
Affiliation:
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Department of Dermatology, Venereology and Leprology, Guru Gobind Singh Medical College and Hospital, Faridkot, Punjab. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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