| Incontinentia pigmenti with ocular involvement: two cases. | |
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MedLine Citation:
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PMID: 22611643 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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Incontinentia pigmenti (IP) is a rare, X-linked dominant disorder that presents at or soon after birth and presents with cutaneous signs and symptoms. Besides its typical skin signs presenting in all patients, central nervous system (CNS), ophthalmologic and dental involvement are encountered as well. In this report, we present two patients at the verrucous stage of IP and review the literature concerning the diagnosis and course of IP. |
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Authors:
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S G Bilgili; A S Karadag; R Karadag; N Akdeniz; G Bulut; O Calka |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Genetic counseling (Geneva, Switzerland) Volume: 23 ISSN: 1015-8146 ISO Abbreviation: Genet. Couns. Publication Date: 2012 |
Date Detail:
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Created Date: 2012-05-22 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9015261 Medline TA: Genet Couns Country: Switzerland |
Other Details:
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Languages: eng Pagination: 57-63 Citation Subset: IM |
Affiliation:
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Department of Dermatology, Yuzuncu Yil University Faculty of Medicine, Van, Turkey. drserapgunes@yahoo.com |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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