Document Detail


Familial occurrence of an association of multiple intestinal atresia and choanal atresia: a new syndrome?
MedLine Citation:
PMID:  19938077     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report on two familial cases from a non-consanguineous marriage, presenting multiple intestinal and choanal atresia. Massive hydramnios and dilatation of the bowel were observed at 29 weeks of gestation during routine ultrasound scan of a healthy mother. The fetal karyotype was normal and cystic fibrosis screening was negative. Regular scans were performed throughout the pregnancy. The child was born at 34 weeks gestation. Choanal atresia was diagnosed at birth and abdominal investigations showed multiple atresia interesting both the small bowel and the colon. Further interventions were necessary because of recurrent obstructions. During the following pregnancy, a dilatation of the fetal intestinal tract was detected by ultrasonography at 27 weeks of gestation. Pregnancy was interrupted. Post-mortem examination of the fetus confirmed the stenosis of long segments of the small intestine associated with areas of colonic atresia. In both cases, histology and distribution were consistent with those reported in hereditary multiple intestinal atresia (HMIA). An association between multiple intestinal and choanal atresia has never been reported. We suggest it could correspond to a new autosomal recessive entity for which cytogenetic investigations and high-resolution array CGH revealed no visible anomalies.
Authors:
Alessandra Ferrarini; Maria-Chiara Osterheld; Yvan Vial; Pierre A de Viragh; Jacques Cotting; Danielle Martinet; Jacques S Beckmann; Florence Fellmann
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  American journal of medical genetics. Part A     Volume:  149A     ISSN:  1552-4833     ISO Abbreviation:  Am. J. Med. Genet. A     Publication Date:  2009 Dec 
Date Detail:
Created Date:  2009-11-30     Completed Date:  2010-01-27     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101235741     Medline TA:  Am J Med Genet A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2661-5     Citation Subset:  IM    
Affiliation:
Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / epidemiology*,  pathology*
Choanal Atresia / complications*,  epidemiology*
Family
Female
Fetus / abnormalities,  pathology
Hair / abnormalities,  ultrastructure
Humans
Infant, Newborn
Intestinal Atresia / complications*,  epidemiology*,  pathology
Male
Pedigree
Pregnancy
Syndrome

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


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