Literature DB >> 31061752

Early-Onset Marfan Syndrome: A Case Series.

Mohanageetha Ardhanari1, Deborah Barbouth2, Sethuraman Swaminathan1.   

Abstract

Mutations in fibrillin 1 cause Marfan syndrome (MFS), an autosomal dominant disorder of the connective tissue, with multisystem manifestations. In early-onset MFS, the physical characteristics are expressed much earlier than the classical MFS. Those affected by this form generally have their mutations restricted to the gene "hotspot" region of exons 24 to 32. Historically, affected individuals usually die within the first few years of life due to heart failure secondary to severe valvular insufficiency. We report three patients with early-onset MFS, whose clinical evolution has been remarkably positive, when compared with other reported cases in the literature.

Entities:  

Keywords:  FBN1 gene ; Marfan syndrome; aortic root dilatation; mitral valve prolapse

Year:  2018        PMID: 31061752      PMCID: PMC6499610          DOI: 10.1055/s-0038-1675338

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  25 in total

1.  Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome.

Authors:  D Bresters; P G Nikkels; E J Meijboom; T M Hoorntje; G Pals; F A Beemer
Journal:  Acta Paediatr       Date:  1999-01       Impact factor: 2.299

Review 2.  The molecular genetics of Marfan syndrome and related microfibrillopathies.

Authors:  P N Robinson; M Godfrey
Journal:  J Med Genet       Date:  2000-01       Impact factor: 6.318

3.  Severe infantile Marfan syndrome versus neonatal Marfan syndrome.

Authors:  Raoul C M Hennekam
Journal:  Am J Med Genet A       Date:  2005-11-15       Impact factor: 2.802

Review 4.  Marfan's syndrome.

Authors:  Daniel P Judge; Harry C Dietz
Journal:  Lancet       Date:  2005-12-03       Impact factor: 79.321

5.  Neonatal Marfan syndrome : in utero presentation with aortic and pulmonary artery dilatation and successful repair of an acute flail mitral valve leaflet in infancy.

Authors:  Prema Ramaswamy; Irena D Lytrivi; Khanh Nguyen; Bruce D Gelb
Journal:  Pediatr Cardiol       Date:  2006-11-07       Impact factor: 1.655

6.  Cardiac transplantation in neonatal Marfan syndrome -- a life-saving approach.

Authors:  T Krasemann; S Kotthoff; H-G Kehl; V Debus; T D T Tjan; C Schmid; J Vogt; H H Scheld
Journal:  Thorac Cardiovasc Surg       Date:  2005-02       Impact factor: 1.827

7.  Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.

Authors:  B Loeys; L Nuytinck; I Delvaux; S De Bie; A De Paepe
Journal:  Arch Intern Med       Date:  2001-11-12

8.  Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40.

Authors:  F Tiecke; S Katzke; P Booms; P N Robinson; L Neumann; M Godfrey; K R Mathews; M Scheuner; G K Hinkel; R E Brenner; H H Hövels-Gürich; C Hagemeier; J Fuchs; F Skovby; T Rosenberg
Journal:  Eur J Hum Genet       Date:  2001-01       Impact factor: 4.246

9.  [Marfan syndrome in the newborn and infants less than 4 months: a series of 9 patients].

Authors:  T Abdel-Massih; A Goldenberg; P Vouhé; F Iserin; P Acar; E Villain; G Agnoletti; D Sidi; D Bonnet
Journal:  Arch Mal Coeur Vaiss       Date:  2002-05

10.  Quadrivalvar replacement in infantile Marfan syndrome.

Authors:  S Strigl; J M Quagebeur; W M Gersony
Journal:  Pediatr Cardiol       Date:  2007-08-08       Impact factor: 1.838

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  1 in total

Review 1.  Cardiomyopathy in Genetic Aortic Diseases.

Authors:  Laura Muiño-Mosquera; Julie De Backer
Journal:  Front Pediatr       Date:  2021-07-15       Impact factor: 3.418

  1 in total

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