| Profuse Congenital Familial Milia with Absent Dermatoglyphics (Basan's Syndrome): Description of a New Family. | |
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MedLine Citation:
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PMID: 21906143 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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Milia are common, small, keratin-containing cysts frequently seen in all age groups. They may arise spontaneously or develop after a variety of stimuli. They can be found alone or as part of syndromes. We present a female neonate born not only with profuse facial milia, but also with acral bullae and absent dermatoglyphics. Similar features were seen in several members of her family. These findings correspond to the syndrome known as Basan's syndrome, a rare autosomal-dominant inherited dermatosis characterized by profuse congenital milia, transient neonatal acral bullae, and absence of dermatoglyphics. |
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Authors:
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Paula Carolina Luna; Margarita Larralde |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2011-9-9 |
Journal Detail:
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Title: Pediatric dermatology Volume: - ISSN: 1525-1470 ISO Abbreviation: - Publication Date: 2011 Sep |
Date Detail:
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Created Date: 2011-9-12 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8406799 Medline TA: Pediatr Dermatol Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Copyright Information:
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© 2011 Wiley Periodicals, Inc. |
Affiliation:
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Dermatology Department, Hospital Alemán, Buenos Aires, Argentina Pediatric Dermatology Section, Hospital Ramos Mejía, Buenos Aires, Argentina. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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