A Report of Two Cases of TGM1 Mutations in Iranian Patients with Lamelar Ichthyosis

ObjectiveAutosomal Recessive Congenital Ichthyosis (ARCI) is a rare, heterogenous keratinization disorder of the skin, classically divided into two clinical subtypes, Lamellar Ichthyosis (LI) and Nonbullous Congenital Ichthyosi-formis Erythroderma (NCIE). Lamellar Ichtyosis is caused by mutations in...

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Bibliographic Details
Main Authors: FARAJI, Abolfazl, MOBARAKI, Maryam, YAZDI, AmirReza, SEYYED HASSANI, Seyyed Mohammad, ARYANI, Omid, HOUSHMAND, Massoud
Format: Online
Language:eng
Published: Iranian Journal of Child Neurology 2011
Online Access:http://journals.sbmu.ac.ir/ijcn/article/view/2123

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