The Clinical and Genetic Characteristics in Children with Idiopathic Hypogonadotropin Hypogonadism.

Qiong ZhouWenbin ShengSuhong YangChao Chun Zou

Published in: Journal of oncology (2022)

It was concluded that variations in the studied genes could lead to the IHH. Ten new variants have been reported which may lead to different symptoms of IHH. For CHD7 variants, the rare sequencing variants (RSVs) of P or LP showed commonly associated with CHARGE syndrome. Findings of the current study may help for the better diagnosis and treatment of IHH.

Keyphrases

copy number
genome wide
young adults
single cell
gene expression
case report
sleep quality
physical activity
depressive symptoms
electron transfer