Document Detail


Endocrine problems in children with Prader-Willi syndrome: special review on associated genetic aspects and early growth hormone treatment.
MedLine Citation:
PMID:  22844316     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder characterized by hypothalamic-pituitary dysfunction. The main clinical features include neonatal hypotonia, distinctive facial features, overall developmental delay, and poor growth in infancy, followed by overeating with severe obesity, short stature, and hypogonadism later in development. This paper reviews recent updates regarding the genetic aspects of this disorder. Three mechanisms (paternal deletion, maternal disomy, and deficient imprinting) are recognized. Maternal disomy can arise because of 4 possible mechanisms: trisomy rescue (TR), gamete complementation (GC), monosomy rescue (MR), and postfertilization mitotic nondisjunction (Mit). Recently, TR/GC caused by nondisjunction at maternal meiosis 1 has been identified increasingly, as a result of advanced maternal childbearing age in Korea. We verified that the d3 allele increases the responsiveness of the growth hormone (GH) receptor to endogenous GH. This paper also provides an overview of endocrine dysfunctions in children with PWS, including GH deficiency, obesity, sexual development, hypothyroidism, and adrenal insufficiency, as well as the effects of GH treatment. GH treatment coupled with a strictly controlled diet during early childhood may help to reduce obesity, improve neurodevelopment, and increase muscle mass. A more active approach to correct these hormone deficiencies would benefit patients with PWS.
Authors:
Dong-Kyu Jin
Related Documents :
160786 - Dental management of the chronically ill child.
19596736 - Predictors of clinical outcomes and hospital resource use of children after tracheotomy.
17142526 - Epidemiology, complications, and cost of hospitalization in children with laboratory-co...
475416 - Adder bites in children.
8106226 - Spectrum of childhood asthma in galway.
9461356 - Natural rubber latex allergy: prevalence and risk factors in patients with spina bifida...
Publication Detail:
Type:  Journal Article     Date:  2012-07-17
Journal Detail:
Title:  Korean journal of pediatrics     Volume:  55     ISSN:  2092-7258     ISO Abbreviation:  Korean J Pediatr     Publication Date:  2012 Jul 
Date Detail:
Created Date:  2012-07-30     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101215374     Medline TA:  Korean J Pediatr     Country:  Korea (South)    
Other Details:
Languages:  eng     Pagination:  224-31     Citation Subset:  -    
Affiliation:
Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Umbilical cord blood transplantation.
Next Document:  Recent incidence of congenital heart disease in neonatal care unit of secondary medical center: a si...