Literature DB >> 3728564

Nonsyndromal anencephaly: possible autosomal recessive variant.

T I Farag, A S Teebi, S A Al-Awadi.   

Abstract

The recurrence of anencephaly in families has been explained on a multifactorial basis. We present two unrelated families with three sibships of several nonsyndromal anencephalics including two pairs of concordantly affected like-sex twins. A rare autosomal recessive variant is proposed and inheritance is discussed in view of parental consanguinity among the two affected sibships in one family.

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Year:  1986        PMID: 3728564     DOI: 10.1002/ajmg.1320240308

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


  5 in total

1.  Meckel syndrome and neural tube defects in Kuwait.

Authors:  A S Teebi; Q A al Saleh; H Odeh
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

2.  Anencephaly: a vanishing problem in Bedouins?

Authors:  T I Farag; S A al-Awadi; S Yassin; T A el-Kassaby; S Jaefary; R Usha; R Uma; S A Mady; M Fakhr; M Mannae
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

3.  The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.

Authors:  G N Kavaslar; S Onengüt; O Derman; A Kaya; A Tolun
Journal:  Am J Hum Genet       Date:  2000-04-04       Impact factor: 11.025

Review 4.  Autosomal recessive disorders among Arabs: an overview from Kuwait.

Authors:  A S Teebi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

5.  Absence of linkage between familial neural tube defects and PAX3 gene.

Authors:  S Chatkupt; F A Hol; Y Y Shugart; M P Geurds; E S Stenroos; M R Koenigsberger; B C Hamel; W G Johnson; E C Mariman
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

  5 in total

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