Glycogen Storage Disease IXc with PHKG2 Mutation and Psoriatic-Like Lesions: A Rare Case

Glycogen storage diseases (GSDs) cause glycogen metabolism disorders in the human body and are genetically determined metabolic illnesses. Due to sufficient glycogen or its diseased states, glycogen is accumulated in the human body tissues due to the enzymatic defect during glycogenolysis/glycogen...

詳細記述

書誌詳細

出版年:	Journal of Liaquat National Hospital
主要な著者:	Shamail Zia, Farozaan Shamail, Fazail Zia, Naeem Uddin, Vardah Zia, Shamsa Naeem, Abdullah Yahya
フォーマット:	論文
言語:	英語
出版事項:	Liaquat National Hospital and Medical College 2025-08-01
主題:	glycogen storage disease phkg2 psoriasis glycogen metabolism autosomal recessive
オンライン･アクセス:	https://journals.lnh.edu.pk/jlnh/pdf/ec55bab5-8b85-4d85-89d9-c83a439d9202.pdf