Literature DB >> 2063908

Epidemiological aspects of Mendelian syndromes in a Spanish population sample: II. Autosomal recessive malformation syndromes.

M L Martínez-Frías1, E Bermejo, A Cereijo, M Sánchez, M López, C Gonzalo.   

Abstract

From April, 1976, to December, 1988, the Spanish Collaborative Study of Congenital Malformations (ECEMC) monitored a total population of 710,815 liveborn infants in 16 of 17 Spanish Regions and identified 14,439 (2.0%) with congenital defects. Among the malformed children, we identified 73 with well recognized autosomal recessive syndromes, for an overall prevalence rate of 10.3 per 100,000 livebirths and a total carrier frequency of 1/49. Considering the Spanish Regions (Comunidades Autónomas), we analyzed the geographical distributions of these syndromes that were homogeneous. We studied the place of birth of the grandparents to determine the distribution of the gene as well as the gene flow.

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Year:  1991        PMID: 2063908     DOI: 10.1002/ajmg.1320380425

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


  2 in total

1.  Impact of prenatal diagnosis by ultrasound on the prevalence of congenital anomalies at birth in southern France.

Authors:  C Julian-Reynier; N Philip; C Scheiner; Y Aurran; F Chabal; A Maron; A Gombert; S Aymé
Journal:  J Epidemiol Community Health       Date:  1994-06       Impact factor: 3.710

2.  The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.

Authors:  Irene Tiemann-Boege; William Navidi; Raji Grewal; Dan Cohn; Brenda Eskenazi; Andrew J Wyrobek; Norman Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-23       Impact factor: 11.205

  2 in total

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