Blau syndrome associated with nucleotide-binding oligomerization domain containing 2 mutation in a baby from Malaysia

Blau syndrome associated with nucleotide-binding oligomerization domain containing 2 mutation in a baby from Malaysia

Blau syndrome (BS) is a very rare autosomal dominant juvenile inflammatory disorder caused by mutation in nucleotide-binding oligomerization domain containing 2 (NOD2). Usually, dermatitis is the first symptom that appears in the 1styear of life. About 220 BS cases with confirmed NOD2 mutation have...

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Bibliographic Details
Main Authors: Kin Fon Leong, Reiko Sato, Glenda Guek Khim Oh, Uttam Surana, Zacharias Aloysius Dwi Pramono
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Indian Journal of Dermatology
Subjects:
Blau syndrome
Malaysia
nucleotide-binding oligomerization domain containing 2
southeast Asia
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2019;volume=64;issue=5;spage=400;epage=403;aulast=Leong

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