Congenital central hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
http://www.nature.com/articles/jp200959.pdf
Reference10 articles.
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2. Windisch W, Hennings E, Storre JH, Matthys H, Sorichter S . Long-term survival of a patient with congenital central hypoventilation syndrome despite lack of continuous ventilatory support. Respiration 2004; 7: 195–198.
3. Weese–Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Silvestri JM, Curran ME et al. Idiopathic congenital central hypoventilation syndrome; analysis of genes pertinent to early autonomic nervous system embryological development and identification of mutations of PHOX2b. Am J Med Genet A 2003; 123: 267–278.
4. Sasaki A, Kanai M, Kijima K, Akaba K, Hashimoto M, Hasegawa H et al. Molecular analysis of congenital central hypoventilation syndrome. Hum Genet 2003; 114: 22–26.
5. Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer DE . Congenital central hypoventilation syndrome: PXOX2B mutations and phenotype. Am J Crit Care Med 2006; 174: 1139–1144.
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1. Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndrome;Clinical Autonomic Research;2022-11-20
2. Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation;Acta Neurologica Belgica;2020-04-25
3. Congenital Central Hypoventilation Syndrome: A Case-Based Learning Opportunity for Neonatal Clinicians;Neonatal Network;2019-07-01
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