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Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics.
J Perinatol. 2009 Oct; 29(10):712-3.JP

Abstract

We report a case of Congenital Central Hypoventilation syndrome (CCHS), diagnosed in utero at 18 weeks' gestation analysis of repeats in the PHOX2b gene in fetal amniocytes and confirmed at delivery. Prenatal diagnosis allowed for serial detailed assessment of fetal breathing characteristics. Fetal breathing in this affected fetus was indistinguishable from breathing characteristics in the non-affected fetus.

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Authors+Show Affiliations

Rajendran GP
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, New York Medical College/Westchester Medical Center, Valhalla, NY, USA.
Kessler MS
No affiliation info available
Manning FA
No affiliation info available

MeSH

AmniocentesisFemaleHomeodomain ProteinsHumansInfant, NewbornMonitoring, AmbulatoryPregnancyPrenatal DiagnosisRespirationSleep Apnea, CentralTranscription FactorsTrinucleotide RepeatsYoung Adult

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

19784002

Citation

Rajendran, G P., et al. "Congenital Central Hypoventilation Syndrome (Ondine's Curse): Prenatal Diagnosis and Fetal Breathing Characteristics." Journal of Perinatology : Official Journal of the California Perinatal Association, vol. 29, no. 10, 2009, pp. 712-3.
Rajendran GP, Kessler MS, Manning FA. Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics. J Perinatol. 2009;29(10):712-3.
Rajendran, G. P., Kessler, M. S., & Manning, F. A. (2009). Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics. Journal of Perinatology : Official Journal of the California Perinatal Association, 29(10), 712-3. https://doi.org/10.1038/jp.2009.59
Rajendran GP, Kessler MS, Manning FA. Congenital Central Hypoventilation Syndrome (Ondine's Curse): Prenatal Diagnosis and Fetal Breathing Characteristics. J Perinatol. 2009;29(10):712-3. PubMed PMID: 19784002.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics. AU - Rajendran,G P, AU - Kessler,M S, AU - Manning,F A, PY - 2009/9/29/entrez PY - 2009/9/29/pubmed PY - 2010/1/29/medline SP - 712 EP - 3 JF - Journal of perinatology : official journal of the California Perinatal Association JO - J Perinatol VL - 29 IS - 10 N2 - We report a case of Congenital Central Hypoventilation syndrome (CCHS), diagnosed in utero at 18 weeks' gestation analysis of repeats in the PHOX2b gene in fetal amniocytes and confirmed at delivery. Prenatal diagnosis allowed for serial detailed assessment of fetal breathing characteristics. Fetal breathing in this affected fetus was indistinguishable from breathing characteristics in the non-affected fetus. SN - 1476-5543 UR - https://www.unboundmedicine.com/medline/citation/19784002/Congenital_Central_Hypoventilation_syndrome__Ondine's_curse_:_prenatal_diagnosis_and_fetal_breathing_characteristics_ L2 - https://doi.org/10.1038/jp.2009.59 DB - PRIME DP - Unbound Medicine ER -