Anesthesia for a child suffering from a deletion in the Xp21 loci resulting in Duchenne disease, glycerol kinase deficiency, and congenital adrenal hypoplasia-Reference-Cited by-同舟云学术

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Anesthesia for a child suffering from a deletion in the Xp21 loci resulting in Duchenne disease, glycerol kinase deficiency, and congenital adrenal hypoplasia

Published:2011-09-01 Issue:10 Volume:21 Page:1085-1087
ISSN:1155-5645
Container-title:Pediatric Anesthesia
language:en
Short-container-title:

Author:

Van Obbergh Luc J.,Corteel Joelle,Papadopoulos Jean,Aunac Sophie

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1460-9592.2011.03634.x/fullpdf

Reference6 articles.

1. Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita;Stuhrmann;Hum Genet,1991

2. Anaesthesia and the sex-linked dystrophies: between a rock and a hard place;Hopkins;Br J Anaesth,2010

3. A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stupor;Ginns;J Pediatr,1984

4. Glycerol kinase deficiency presenting with hypodipsia, osmotic diuresis and severe hypernatremia;Mak;J Inherit Metab Dis,2005

5. Human glycerol kinase deficiency with hyperglycerolemia and glyceroluria;McCabe;Biochem Biophys Res Commun,1977

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Complex Glycerol Kinase Deficiency (Xp21 Deletion Syndrome): A Case Report of a Contiguous Gene Disorder Necessitating Creative Anesthetic Planning;A&A Practice;2020-08

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