Kindler syndrome: A rare case report

Kindler syndrome: A rare case report

Kindler syndrome is a very rare genodermatosis with an autosomal recessive pattern and about 250 cases have been reported worldwide. The mutant gene is Fermitin family homolog 1 gene (KIND1), located on chromosome 20p12.3, which encodes for focal adhesion protein “Fermitin family homologue 1 protein...

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Bibliographic Details
Main Authors: Shweta Satyanarayan Kandikatla, Shylaja Someshwar, Pranjal Ahire
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2021-01-01
Series:Muller Journal of Medical Sciences and Research
Subjects:
caenorhabditis
kindler
poikiloderma
Online Access:http://www.mjmsr.net/article.asp?issn=0975-9727;year=2021;volume=12;issue=1;spage=52;epage=55;aulast=Kandikatla

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http://www.mjmsr.net/article.asp?issn=0975-9727;year=2021;volume=12;issue=1;spage=52;epage=55;aulast=Kandikatla

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