Literature DB >> 24770546

Aarskog-Scott syndrome: a novel mutation in the FGD1 gene associated with severe craniofacial dysplasia.

Christiane Völter1, Ramón Martínez, Rudolf Hagen, Wolfram Kress.   

Abstract

UNLABELLED: Aarskog syndrome (AAS) is an X-linked human disease that affects the skeletal formation and embryonic morphogenesis and is caused by mutations in the FGD1 gene. Patients typically show distinctive skeletal and genital developmental abnormalities, but a broad spectrum of clinical phenotypes has been observed. We report here on the clinical and molecular analysis of a family that reveals a novel FGD1 mutation in a 9-year-old boy displaying extreme craniofacial dysplasia associated with attention deficit hyperactivity disorder. Sequencing of FGD1 revealed a novel mutation in exon 7 at position c.1468 C > T in the index patient, leading to a stop codon in the highly conserved RhoGEF gene domain. His mother and maternal grandmother were also found to be heterozygous for this FGD1 mutation.
CONCLUSION: Our results identify a novel mutation of FDG1 in a family with Aarskog syndrome and underscore the phenotypical variability of this condition.

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Year:  2014        PMID: 24770546     DOI: 10.1007/s00431-014-2317-3

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  17 in total

1.  Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome.

Authors:  C E Schwartz; G Gillessen-Kaesbach; M May; M Cappa; J Gorski; K Steindl; G Neri
Journal:  Eur J Hum Genet       Date:  2000-11       Impact factor: 4.246

2.  Neurobehavioral disorders in patients with Aarskog-Scott syndrome affected by novel FGD1 mutations.

Authors:  Tadashi Kaname; Kumiko Yanagi; Nobuhiko Okamoto; Kenji Naritomi
Journal:  Am J Med Genet A       Date:  2006-06-15       Impact factor: 2.802

3.  Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q).

Authors:  Alfredo Orrico; Lucia Galli; Sabrina Buoni; Giuseppe Hayek; Anna Luchetti; Stefania Lorenzini; Michele Zappella; Maria Grazia Pomponi; Vincenzo Sorrentino
Journal:  Am J Med Genet A       Date:  2005-05-15       Impact factor: 2.802

4.  X-linked Aarskog syndrome: report on a novel FGD1 gene mutation. Executive dysfunction as part of the behavioural phenotype.

Authors:  W M A Verhoeven; J I M Egger; A J M Hoogeboom
Journal:  Genet Couns       Date:  2012

5.  Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

Authors:  R R Lebel; M May; S Pouls; H A Lubs; R E Stevenson; C E Schwartz
Journal:  Clin Genet       Date:  2002-02       Impact factor: 4.438

6.  Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene.

Authors:  A Orrico; L Galli; L Faivre; J Clayton-Smith; S M Azzarello-Burri; J M Hertz; S Jacquemont; R Taurisano; I Arroyo Carrera; E Tarantino; K Devriendt; D Melis; T Thelle; U Meinhardt; V Sorrentino
Journal:  Am J Med Genet A       Date:  2010-02       Impact factor: 2.802

7.  A novel mutation in a mother and a son with Aarskog-Scott syndrome.

Authors:  Ayça Altıncık; Tadashi Kaname; Korcan Demir; Ece Böber
Journal:  J Pediatr Endocrinol Metab       Date:  2013       Impact factor: 1.634

8.  [The assessment of Attention Deficit Hyperactivity Disorder (ADHD) by teacher ratings - validity and reliability of the FBB-HKS].

Authors:  Dieter Breuer; Tanja Wolff Metternich; Manfred Döpfner
Journal:  Z Kinder Jugendpsychiatr Psychother       Date:  2009-09

9.  Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor.

Authors:  N G Pasteris; A Cadle; L J Logie; M E Porteous; C E Schwartz; R E Stevenson; T W Glover; R S Wilroy; J L Gorski
Journal:  Cell       Date:  1994-11-18       Impact factor: 41.582

10.  Unilateral focal polymicrogyria in a patient with classical Aarskog-Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1.

Authors:  Armand Bottani; Alfredo Orrico; Lucia Galli; Olivier Karam; Charles-André Haenggeli; Solène Ferey; Bernard Conrad
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

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  4 in total

1.  Identification of novel mutations in Mexican patients with Aarskog-Scott syndrome.

Authors:  Mariana Pérez-Coria; José J Lugo-Trampe; Michell Zamudio-Osuna; Iram P Rodríguez-Sánchez; Angel Lugo-Trampe; Beatriz de la Fuente-Cortez; Luis D Campos-Acevedo; Laura E Martínez-de-Villarreal
Journal:  Mol Genet Genomic Med       Date:  2015-02-17       Impact factor: 2.183

2.  Novel variant in the FGD1 gene causing Aarskog-Scott syndrome.

Authors:  Yihua Ge; Niu Li; Zhigang Wang; Jian Wang; Haiqing Cai
Journal:  Exp Ther Med       Date:  2017-04-05       Impact factor: 2.447

Review 3.  The Prevalence of Clinical Features in Patients with Aarskog-Scott Syndrome and Assessment of Genotype-Phenotype Correlation: A Systematic Review.

Authors:  Victor Zanetti Drumond; Lucas Sousa Salgado; Camila Sousa Salgado; Vitor Augusto de Lima Oliveira; Eliene Magda de Assis; Michel Campos Ribeiro; Analina Furtado Valadão; Alfredo Orrico
Journal:  Genet Res (Camb)       Date:  2021-02-02       Impact factor: 1.588

4.  A novel frameshift mutation in the FGD1 gene causing Aarskog-Scott syndrome patient with hypogonadism: a case report.

Authors:  Hongshuai Jia; Tiantian Ma; Ziqin Liu; Yuru Ouyang; Chunsheng Hao
Journal:  Transl Pediatr       Date:  2021-05
  4 in total

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