Congenital diaphragmatic hernia in a case of Cat eye syndrome

Author:

Alsat Ebru Aileen1ORCID,Reutter Heiko12,Bagci Soyhan1,Kipfmueller Florian1,Engels Hartmut2,Raff Ruth2,Mangold Elisabeth2,Gembruch Ulrich3,Geipel Annegret3,Müller Andreas1,Schaible Thomas4

Affiliation:

1. Department of Neonatology and Pediatric Intensive Care; University of Bonn; Bonn Germany

2. Institute of Human Genetics; University of Bonn; Bonn Germany

3. Department of Obstetrics and Prenatal Medicine; University of Bonn; Bonn Germany

4. Department of Neonatology; University Medicine Mannheim; University of Heidelberg; Mannheim Germany

Publisher

Wiley

Subject

General Medicine

Reference21 articles.

1. Phenotypic variability of Cat-Eye syndrome;Berends;Genet Couns,2001

2. The “cat eye” syndrome-report of a case with hypothyroidism;Ioan;Endocrinologie,1986

3. The “cat eye syndrome”: dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture;Schinzel;Hum Genet,1981

4. Wide clinical variability in cat eye syndrome patients: four non-related patients and three patients from the same family;Belangero;Cytogenet Genome Res,2012

5. A new case of a severe clinical phenotype of the cat-eye syndrome;Denavit;Genet Couns,2004

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