Literature DB >> 2063907

Epidemiological aspects of Mendelian syndromes in a Spanish population sample: I. Autosomal dominant malformation syndromes.

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

Abstract

Using a sample of 710,815 liveborn infants throughout Spain, monitored from April, 1976, to December, 1988, by the Spanish Collaborative Study of Congenital Malformations (ECEMC), we estimated the prevalence of each recognized autosomal dominant malformation syndrome for a total prevalence figure of 12.1 per 100,000 live births, including all detected autosomal dominant malformations syndromes. We estimated that the mutation rate for those syndromes was 48.5 per 1,000,000 gametes. The geographical distribution of these syndromes was homogeneous in the Spanish Regions.

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Year:  1991        PMID: 2063907     DOI: 10.1002/ajmg.1320380424

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


  6 in total

1.  Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 gene.

Authors:  M J Trujillo-Tiebas; M Fenollar-Cortés; I Lorda-Sánchez; J Díaz-Recasens; A Carrillo Redondo; C Ramos-Corrales; C Ayuso
Journal:  J Assist Reprod Genet       Date:  2009-09-30       Impact factor: 3.412

2.  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

3.  A silent epidemic of major congenital malformations in Tigray, northern Ethiopia: hospital-based study.

Authors:  Hayelom Kebede Mekonen; Yibrah Berhe; Birhane Alem Berihu; Hale Teka; Abera Hadgu; Letekirstos Gebregziabher; Etenat Halefom Berhe; Tony Magana; Afework Mulugeta
Journal:  Sci Rep       Date:  2021-10-26       Impact factor: 4.379

4.  Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases.

Authors:  Munis Dundar; Asli Subasioglu Uzak; Murat Erdogan; Yagut Akbarova
Journal:  EPMA J       Date:  2011-05-06       Impact factor: 6.543

5.  Pattern of congenital anomalies in newborn: a hospital-based study.

Authors:  Mohamed A El Koumi; Ehab A Al Banna; Ibrahim Lebda
Journal:  Pediatr Rep       Date:  2013-02-05

6.  Birth prevalence of achondroplasia: A systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Femke van Kessel; Rosa van Hoorn; Judith van den Bosch; Renée Shediac; Sarah Landis
Journal:  Am J Med Genet A       Date:  2020-08-17       Impact factor: 2.802

  6 in total

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