Identification of a Novel C16orf57 Mutation in Iranian Patient with Clericuzio-type Poikiloderma with Neutropenia (CPN): A Case Report

Identification of a Novel C16orf57 Mutation in Iranian Patient with Clericuzio-type Poikiloderma with Neutropenia (CPN): A Case Report

Poikiloderma is a hereditary pathologic situation in which the appearance of skin rash is associated with epidermal atrophy, telangiectasia, and reticular dyspigmentation skin symptoms of poikiloderma are usually caused by sun damage. The main reason forpoikiloderma is unknown. We introduce a 14- m...

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Bibliographic Details
Main Authors: Farhad Abolnezhadian, Sara Iranparast
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2019-08-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Hepatoslenomegaly
Poikiloderma
Thrombocytopenia
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2261

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