Genetics of Growth Hormone Deficiency
Journal Title: Journal of Clinical Research in Pediatric Endocrinology - Year 2009, Vol 1, Issue 1
Abstract
From the initiation of the primordium to the expression of mature growth hormone (GH)1 gene, a variety of genes, transcription factors, signalling pathways, and epigenetic control factors take part in the embryological development of the anterior hypophyseal somatotrophic cells. A defect in this process may result in multiple pituitary deficiency or isolated growth hormone deficiency depending on the temporal or spatial position of the individual factor. This article reviews these factors in a chronological order. This review presents some of these genetic mutations that result in obesity. DOI: 10.4008/jcrpe.v1i1.30
Authors and Affiliations
Ali Topaloğlu
Prevalence of Cryptorchidism Among Bulgarian Boys
Background: Cryptorchidism is the most common congenital defect of the male urogenital system. It may be an important cause for male infertility. The data about its prevalence in South-eastern European countries and espe...
Foreword
In presenting this first issue of the Journal of Clinical Research in Pediatric Endocrinology (JCRPE), we renew our hopes that in due time this journal will establish its place in the international arena of Pediatric End...
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Nutrition plays a fundamental role in determining the growth of individuals. An appropriate growth progression is considered a harbinger of adequate nutrient intake and good health. On the other hand growth deceleration...
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Most steroid disorders of the adrenal cortex come to clinical attention in childhood and in order to investigate these problems, there are many challenges to the laboratory which need to be appreciated to a certain exten...
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