Genetic Anomalies of Growth Hormone Deficiency in Pediatrics.


Journal

Endocrine, metabolic & immune disorders drug targets
ISSN: 2212-3873
Titre abrégé: Endocr Metab Immune Disord Drug Targets
Pays: United Arab Emirates
ID NLM: 101269157

Informations de publication

Date de publication:
2021
Historique:
received: 21 12 2019
revised: 27 03 2020
accepted: 15 05 2020
pubmed: 6 7 2020
medline: 27 10 2021
entrez: 5 7 2020
Statut: ppublish

Résumé

Several different proteins regulate, directly or indirectly, the production of growth hormones from the pituitary gland, thereby complex genetics is involved. Defects in these genes are related to the deficiency of growth hormones solely, or deficiency of other hormones, secreted from the pituitary gland including growth hormones. These studies can aid clinicians to trace the pattern of the disease between the families, start early treatment and predict possible future consequences. This paper highlights some of the most common and novel genetic anomalies concerning growth hormones, which are responsible for various genetic defects in isolated growth and combined pituitary hormone deficiency disease.

Identifiants

pubmed: 32621723
pii: EMIDDT-EPUB-107903
doi: 10.2174/1871530320666200704144912
doi:

Substances chimiques

Human Growth Hormone 12629-01-5

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

288-297

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Majid Firouzi (M)

Department of Pediatrics, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.

Hamidreza Sherkatolabbasieh (H)

Department of Pediatrics, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.

Shiva Shafizadeh (S)

Department of Internal Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.

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Classifications MeSH