Literature DB >> 20684000

Mental retardation, growth retardation, unusual nose, and open mouth: an autosomal recessive entity.

Fowzan S Alkuraya1.   

Abstract

In this paper, I describe the investigations in three members of an extended consanguineous family from Saudi Arabia, in which nine members show severe mental retardation, long eyelashes, high nasal bridge, underdeveloped malae, low hanging columella, thin upper vermillion, and everted lower vermillion, retrognathia, and an open mouth apparently caused by mandibular dentoalveolar protrusion. Pedigree analysis makes it likely that this is an autosomal recessively inherited disorder. A detailed literature search failed to show a similar entity. Copyright 2010 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2010        PMID: 20684000     DOI: 10.1002/ajmg.a.33575

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH.

Authors:  Ranad Shaheen; Zuhair Rahbeeni; Amal Alhashem; Eissa Faqeih; Qi Zhao; Yong Xiong; Agaadir Almoisheer; Sarah M Al-Qattan; Halima A Almadani; Noufa Al-Onazi; Badi S Al-Baqawi; Mohammad Ali Saleh; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2014-05-15       Impact factor: 11.025

2.  Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort.

Authors:  Ranad Shaheen; Nisha Patel; Hanan Shamseldin; Fatema Alzahrani; Ruah Al-Yamany; Agaadir ALMoisheer; Nour Ewida; Shamsa Anazi; Maha Alnemer; Mohamed Elsheikh; Khaled Alfaleh; Muneera Alshammari; Amal Alhashem; Abdullah A Alangari; Mustafa A Salih; Martin Kircher; Riza M Daza; Niema Ibrahim; Salma M Wakil; Ahmed Alaqeel; Ikhlas Altowaijri; Jay Shendure; Amro Al-Habib; Eissa Faqieh; Fowzan S Alkuraya
Journal:  Genet Med       Date:  2015-12-03       Impact factor: 8.822

3.  Immune dysfunction in MGAT2-CDG: A clinical report and review of the literature.

Authors:  Sheri A Poskanzer; Matthew J Schultz; Coleman T Turgeon; Noemi Vidal-Folch; Kris Liedtke; Devin Oglesbee; Dimitar K Gavrilov; Silvia Tortorelli; Dietrich Matern; Piero Rinaldo; James T Bennett; Jenny M Thies; Irene J Chang; Anita E Beck; Kimiyo Raymond; Eric J Allenspach; Christina Lam
Journal:  Am J Med Genet A       Date:  2020-10-12       Impact factor: 2.802

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.