Literature DB >> 15690380

Natural history of cardiac involvement in geleophysic dysplasia.

A Scott1, S Yeung, D F Dickinson, G Karbani, Y J Crow.   

Abstract

Geleophysic dysplasia is an autosomal recessive short-limbed, dysmorphic syndrome. The condition is frequently associated with cardiac valvular disease, which may result in secondary hypertrophy and cardiac failure. We describe two distantly related Pakistani children with classical features of geleophysic dysplasia. Pulmonary stenosis was recognized in both within a few months of birth. The younger child shows no signs of cardiac decompensation at the age of 7 years whilst her older cousin has developed a significant pulmonary gradient requiring surgical intervention in the second decade of life. The natural history of his disorder highlights that the cardiac involvement seen in apparently stable forms of geleophysic dysplasia is frequently progressive. (c) 2004 Wiley-Liss, Inc.

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Year:  2005        PMID: 15690380     DOI: 10.1002/ajmg.a.30450

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


  5 in total

1.  Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia.

Authors:  Christiaan de Bruin; Courtney Finlayson; Mariana F A Funari; Gabriela A Vasques; Bruna Lucheze Freire; Antonio M Lerario; Melissa Andrew; Vivian Hwa; Andrew Dauber; Alexander A L Jorge
Journal:  Horm Res Paediatr       Date:  2016-06-02       Impact factor: 2.852

2.  Three novel mutations of the FBN1 gene in Chinese children with acromelic dysplasia.

Authors:  Yu Wang; Huiwen Zhang; Jun Ye; Lianshu Han; Xuefan Gu
Journal:  J Hum Genet       Date:  2014-08-21       Impact factor: 3.172

3.  Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia.

Authors:  Slimane Allali; Carine Le Goff; Isabelle Pressac-Diebold; Gwendoline Pfennig; Clémentine Mahaut; Nathalie Dagoneau; Yasemin Alanay; Angela F Brady; Yanick J Crow; Koen Devriendt; Valérie Drouin-Garraud; Elisabeth Flori; David Geneviève; Raoul C Hennekam; Jane Hurst; Deborah Krakow; Martine Le Merrer; Klaske D Lichtenbelt; Sally A Lynch; Stanislas Lyonnet; Kay MacDermot; Sahar Mansour; André Megarbané; Heloisa G Santos; Miranda Splitt; Andrea Superti-Furga; Sheila Unger; Denise Williams; Arnold Munnich; Valérie Cormier-Daire
Journal:  J Med Genet       Date:  2011-03-17       Impact factor: 6.318

4.  The Clinical Cases of Geleophysic Dysplasia: One Gene, Different Phenotypes.

Authors:  Evgenia Globa; Nataliya Zelinska; Andrew Dauber
Journal:  Case Rep Endocrinol       Date:  2018-07-03

5.  A Review of Three Chinese Cases of Acromicric/Geleophysic Dysplasia with FBN1 Mutations.

Authors:  Yan-Chun Shan; Zhao-Chuan Yang; Liang Ma; Ni Ran; Xue-Ying Feng; Xiao-Mei Liu; Peng Fu; Ming-Ji Yi
Journal:  Int J Gen Med       Date:  2021-05-17
  5 in total

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