Literature DB >> 8074149

Seckel syndrome in a Yemeni family in Saudi Arabia.

A G Krishna1, E M Scrimgeour, T H Zawawi.   

Abstract

We studied a 28-year-old Yemeni woman with typical Seckel syndrome. Two deceased sibs, a twin sister and a brother, had also been affected. The father of these individuals was married to his cousin's daughter: the pedigree suggests autosomal recessive inheritance. Classical Seckel syndrome has not been reported previously in Arabs, and this appears to be the first report from the Middle East.

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Year:  1994        PMID: 8074149     DOI: 10.1002/ajmg.1320510310

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


  3 in total

1.  Seckel-like syndrome or Seckel variants?

Authors:  Mathew Punnachalil Cherian
Journal:  Ann Saudi Med       Date:  2004 Nov-Dec       Impact factor: 1.526

2.  Palatoplasty in a patient with Seckel syndrome.

Authors:  Ramneesh Garg; Sanjeev Uppal; Rajinder Mittal; Anju Grewal; Dinesh Sood; Sheerin Shah
Journal:  Ann Maxillofac Surg       Date:  2012-01

3.  Central nervous system vasculopathy and Seckel syndrome: case illustration and systematic review.

Authors:  Osama Khojah; Saeed Alamoudi; Nouf Aldawsari; Mohammed Babgi; Ahmed Lary
Journal:  Childs Nerv Syst       Date:  2021-08-03       Impact factor: 1.475

  3 in total

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