Document Detail


Possible nagashima-type palmoplantar keratosis in two siblings.
MedLine Citation:
PMID:  23626539     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Nagashima-type palmoplantar keratosis (PPK) is an autosomal recessive, transgressive and non-progressive form of PPK. It was once described as a mild form of mal de Meleda, but it is now proposed as a novel entity of PPK. Since its pathogenesis remains unclear, it is important to clarify the mode of inheritance. Here, we present a case of possible Nagashima-type PPK in 2 siblings. The siblings had non-affected parents, suggesting that the mode of inheritance was autosomal recessive. At present, reports on PPK in the English literature are limited, and thus the clinical features of Nagashima-type PPK may not be well appreciated in Western countries. More reports and concise clinical observations with genetic studies are required to establish this new entity of PPK.
Authors:
Kio Park; Kenji Kabashima; Yoshiki Miyachi
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Publication Detail:
Type:  Journal Article     Date:  2013-03-04
Journal Detail:
Title:  Case reports in dermatology     Volume:  5     ISSN:  1662-6567     ISO Abbreviation:  Case Rep Dermatol     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-04-29     Completed Date:  2013-04-30     Revised Date:  2013-05-02    
Medline Journal Info:
Nlm Unique ID:  101517685     Medline TA:  Case Rep Dermatol     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  58-60     Citation Subset:  -    
Affiliation:
Department of Dermatology, Yamato Takada Municipal Hospital, Nara, Kyoto, Japan.
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