Isolated growth hormone deficiency

Libia M. Hernálndez, Phillip D.K. Lee, Cecilia Camacho-Hübner

Research output: Contribution to journalReview article

31 Scopus citations

Abstract

Isolated growth hormone deficiency (IGHD) represents conditions of GH deficiency that are not necessarily associated with other pituitary hormone deficiencies or with an organic lesion. Three sub-categories of IGHD have been clinically identified (IGHD types 1-3), and IGHD type 1 has been further separated into IGHD types 1a and b. However, this clinical sub-categorization of IGHD may need reconsideration due to the recent identification of molecular heterogeneity within each sub-type of IGHD. In a small number of children with IGHD, defects in the GH, GH-releasing hormone receptor (GHRH-R), and GH1 genes have been identified. In most cases, no cause for IGHD can be identified; however, the proportion of idiopathic IGHD cases may be decreasing due to identification of causative factors. The phenotype of IGHD is variable depending in part on the underlying genetic disorders in the affected individuals. Several studies have focused on the usefulness of MRI findings in patients with GHD but anatomic abnormalities of the pituitary gland are variable. We review current studies and the clinical, biochemical, and molecular features described for different groups of affected individuals with IGHD.

Original languageEnglish (US)
Pages (from-to)351-357
Number of pages7
JournalPituitary
Volume10
Issue number4
DOIs
StatePublished - Dec 2007

Keywords

  • Growth hormone
  • Growth hormone deficiency
  • Growth hormone releasing hormone
  • Pituitary

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

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    Hernálndez, L. M., Lee, P. D. K., & Camacho-Hübner, C. (2007). Isolated growth hormone deficiency. Pituitary, 10(4), 351-357. https://doi.org/10.1007/s11102-007-0073-3