Literature DB >> 16700088

Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.

Isabel López1, Juan A Bafalliu, M Carmen Bernabé, Francisco García, Miguel Costa, Encarna Guillén-Navarro.   

Abstract

OBJECTIVE: To show the importance of using high-resolution chromosome analysis and FISH-technique for finding subtle chromosomal lesions in prenatal diagnosis specially when there are abnormal ultrasound findings.
METHODS: Ecographic examination of the fetus. GTG banded chromosome and FISH analysis using subtelomeric probes on amniocytes.
RESULTS: We report two prenatal cases with congenital diaphragmatic hernia (CDH) and congenital heart defects (CHDs) with different deletions confirmed by FISH: del(8)(p23.1p23.1) and del(15)(q26.1).
CONCLUSION: These cases support the evidence that the regions 15q26.1 and 8p23.1 may play an important role in the development of the diaphragm. A deletion 8p23.1 or 15q26.1 should be considered whenever a CDH and/or a cardiac abnormality are detected on ultrasound. Copyright 2006 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2006        PMID: 16700088     DOI: 10.1002/pd.1468

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  14 in total

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Review 5.  Genetic factors in congenital diaphragmatic hernia.

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6.  Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

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Review 8.  Genetic aspects of human congenital diaphragmatic hernia.

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10.  Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review.

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