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Description

Yin et al., 2012

Front Pharmacol 2022;13:876469

Content is produced for educational purposes and does not constitute a clinical recommendation, prescription, or endorsement of any specific product or protocol

Disorders of GH in childhood is outlined in the Endotext chapter Disorders of Growth Hormone in Childhood by Murray and Clayton (132) Primary IGF-I deficiency or GH insensitivity is severe in homozygous genetic defects in genes including the GH receptor (Laron syndrome) gene, STAT-5b gene and IGF-I gene