Isolated growth hormone deficiency type IA due to a novel GH1 variant: a case report

• Main Authors: Xi Yang (Author), Mingming Yuan (Author), Zhuoguang Li (Author), Yanqin Ying (Author), Ling Hou (Author), Xiaoping Luo (Author)
• Format: Book
• Published: BMC, 2021-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background A case of isolated growth hormone deficiency type IA (IGHD IA) caused by novel compound heterozygous mutation in the GH1 gene was reported in this study, which aimed to provide insights that will benefit future diagnosis and treatment. Case presentation We analyzed and summarized...