Natural history of growth hormone receptor deficiency

Citation
Al. Rosenbloom et al., Natural history of growth hormone receptor deficiency, ACT PAEDIAT, 88, 1999, pp. 153-156
Citations number
18
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
ACTA PAEDIATRICA
ISSN journal
08035253 → ACNP
Volume
88
Year of publication
1999
Supplement
428
Pages
153 - 156
Database
ISI
SICI code
0803-5253(199902)88:<153:NHOGHR>2.0.ZU;2-H
Abstract
This review discusses the natural history of growth hormone receptor defici ency (GHRD) in relation to epidemiology, mortality, growth, certain aspects of body composition, and intellectual development. The majority of affecte d individuals are of Semitic origin and 90% come from the Indian peninsula, the Middle East, or elsewhere in the Mediterranean. There is a twofold inc reased mortality before the age of 7 years for children with GHRD. Affected adults may have increased cardiovascular risk resulting from increased tot al cholesterol and low-density lipoprotein cholesterol, unrelated to adipos ity or insulin resistance. Intrauterine growth is affected minimally, if at all. Within a genetically homogeneous population in Ecuador, postnatal gro wth effects are as variable as in a large genetically heterogeneous populat ion. There is no influence of parental heights. Areal bone mineral density is reduced in adults with GHRD, but estimated volumetric bone density (bone mineral apparent density) is normal. Intellectual development is unaffecte d by GHRD.