Literature DB >> 4003435

A family study of congenital diaphragmatic defects.

A Czeizel, M Kovács.   

Abstract

The occurrence of specific and nonspecific congenital anomalies was determined in first degree relatives of index patients with congenital diaphragmatic defects who were born in Hungary between 1970 and 1979 and were ascertained through a population-based registry. The cases were grouped into Bochdalek types (N = 156), other types (N = 26), unclassified types (N = 55), and multiple congenital anomalies (MCA) cases including those with congenital diaphragmatic defects (N = 96). The sib occurrence in the Bochdalek type was 0.9% (taking into consideration also the unclassified cases or the total material, it was 0.5% or 0.4%, respectively). Specific familial clusters were not found in other types. Neural tube defects were detected in 1.8% of sibs in the total material and 2.4% in MCA cases.

Entities:  

Mesh:

Year:  1985        PMID: 4003435     DOI: 10.1002/ajmg.1320210115

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  14 in total

1.  Congenital diaphragmatic hernia with probable autosomal recessive inheritance in an extended consanguineous Pakistani pedigree.

Authors:  S J Mitchell; T Cole; D H Redford
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Spina bifida and hydrocephalus: a population study over a 35-year period.

Authors:  S J Bamforth; P A Baird
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

3.  The epidemiology of diaphragmatic hernia.

Authors:  E Robert; B Källén; J Harris
Journal:  Eur J Epidemiol       Date:  1997-09       Impact factor: 8.082

4.  Familial occurrence of congenital diaphragmatic hernia : Father-to-son inheritance.

Authors:  J P Janik; J S Janik; E R Wayne; A Pantoja
Journal:  Pediatr Surg Int       Date:  2013-09-21       Impact factor: 1.827

5.  A population-based case-control teratologic study of oral dipyrone treatment during pregnancy.

Authors:  Ferenc Bánhidy; Nándor Acs; Erzsébet Puhó; Andrew E Czeizel
Journal:  Drug Saf       Date:  2007       Impact factor: 5.606

6.  Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program.

Authors:  Barbara R Pober; Angela Lin; Meaghan Russell; Kate G Ackerman; Sharmila Chakravorty; Bernarda Strauss; Marie Noel Westgate; Jay Wilson; Patricia K Donahoe; Lewis B Holmes
Journal:  Am J Med Genet A       Date:  2005-10-01       Impact factor: 2.802

7.  A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.

Authors:  Cammon B Arrington; Steven B Bleyl; Nori Matsunami; Neil E Bowles; Tami I Leppert; Bradley L Demarest; Karen Osborne; Bradley A Yoder; Janice L Byrne; Joshua D Schiffman; Donald M Null; Robert DiGeronimo; Michael Rollins; Roger Faix; Jessica Comstock; Nicola J Camp; Mark F Leppert; H Joseph Yost; Luca Brunelli
Journal:  Am J Med Genet A       Date:  2012-11-19       Impact factor: 2.802

8.  Split hand, obstructive urinary anomalies and spina bifida or diaphragmatic defect syndrome with autosomal dominant inheritance.

Authors:  A Czeizel; A Losonci
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

9.  Epidemiological study of congenital diaphragmatic defects with special reference to aetiology.

Authors:  N Philip; D Gambarelli; J M Guys; J Camboulives; S Ayme
Journal:  Eur J Pediatr       Date:  1991-08       Impact factor: 3.183

Review 10.  Genetic aspects of human congenital diaphragmatic hernia.

Authors:  B R Pober
Journal:  Clin Genet       Date:  2008-05-28       Impact factor: 4.438

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