Case 1: A Term Male Infant with Hypoglycemia and Hyperbilirubinemia as Initial Presentation
Author:
Affiliation:
1. Departments of Pediatrics and
2. Neonatology, Dell Children’s Medical School of Central Texas, Austin, TX
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology, and Child Health
Link
https://publications.aap.org/neoreviews/article-pdf/21/4/e264/822653/neoreviews_042019iositn00047.pdf
Reference8 articles.
1. An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita;Zanaria;Nature,1994
2. Identification of a novel mutation of NR0B1 in a patient with X-linked adrenal hypoplasia and symptomatic treatment;Yang;J Pediatr Endocrinol Metab,2017
3. Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome;Cole;Clin Chem,1994
4. Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion;Bartley;J Pediatr,1986
5. Molecular mechanisms of DAX1 action;Iyer;Mol Genet Metab,2004
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