Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Isolated growth hormone deficiency type 2

Isolated growth hormone deficiency type 2 is an autosomal dominant disorder caused by mutations of the GH1 gene. Clinically this disorder is characterized by growth retardation and delayed bone maturation. The disease can be managed by supplementation of growth hormone.

Systematic

Growth hormone deficiency
GH1
Growth hormone secretagogue resistance
Isolated growth hormone deficiency type 1A
Isolated growth hormone deficiency type 1B
Isolated growth hormone deficiency type 2
GH1
Isolated growth hormone deficiency type 3
Kowarski syndrome
Update:
Copyright © 2005-2020 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944
Sitemap | Webmail | Disclaimer | Privacy Issues