Document Detail


Incontinentia pigmenti with ocular involvement: two cases.
MedLine Citation:
PMID:  22611643     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
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.
Authors:
S G Bilgili; A S Karadag; R Karadag; N Akdeniz; G Bulut; O Calka
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Genetic counseling (Geneva, Switzerland)     Volume:  23     ISSN:  1015-8146     ISO Abbreviation:  Genet. Couns.     Publication Date:  2012  
Date Detail:
Created Date:  2012-05-22     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9015261     Medline TA:  Genet Couns     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  57-63     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Yuzuncu Yil University Faculty of Medicine, Van, Turkey. drserapgunes@yahoo.com
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