Literature DB >> 3728560

Prevalence of mitral-valve prolapse in the Stickler syndrome.

R M Liberfarb, A Goldblatt.   

Abstract

An increased prevalence of mitral-valve prolapse occurs in several connective tissue dysplasias, including Marfan syndrome, Ehlers-Danlos syndrome, and pseudoxanthoma elasticum. We evaluated 57 patients diagnosed as having the Stickler syndrome for mitral-valve prolapse by auscultation and two-dimensional echocardiography. The diagnosis was made on the basis of craniofacial and musculoskeletal abnormalities, sensorineural hearing loss, eye defects, and a family history of Stickler syndrome. Twenty-six patients (45.6%) had mitral-valve prolapse, including 11 of 22 females (50.0%) and 15 of 35 males (42.9%). The age range of our study population was 4 to 60 years. Prevalence of mitral-valve prolapse did not increase with age. Nine patients (34.6% of those with mitral-valve prolapse) had the click-murmur syndrome; only one of them was symptomatic. Because of the growing list of complications associated with mitral-valve prolapse, all patients with Stickler syndrome should be evaluated by auscultation, electrocardiogram, and echocardiography. Those with mitral-valve prolapse should be advised to have periodic follow-up and to instruct physicians caring for them of their need for antibiotic prophylaxis with certain surgical procedures.

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Year:  1986        PMID: 3728560     DOI: 10.1002/ajmg.1320240302

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


  11 in total

1.  Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome.

Authors:  Thomas Theelen; Sioe Lie Go; Maurits A D Tilanus; B Jeroen Klevering; August F Deutman; Frans P M Cremers; Carel B Hoyng
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-04-02       Impact factor: 3.117

2.  Unusual occurrence of cervical myelopathy in a case of Stickler's syndrome.

Authors:  S Noël; D Balériaux; N Telerman-Toppet
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

3.  Stickler's syndrome.

Authors:  I K Temple
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 4.  Clinical and Molecular genetics of Stickler syndrome.

Authors:  M P Snead; J R Yates
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

5.  Temporal and spatial expression of collagens during murine atrioventricular heart valve development and maintenance.

Authors:  Jacqueline D Peacock; Yinhui Lu; Manuel Koch; Karl E Kadler; Joy Lincoln
Journal:  Dev Dyn       Date:  2008-10       Impact factor: 3.780

Review 6.  Genetics of valvular heart disease.

Authors:  Stephanie LaHaye; Joy Lincoln; Vidu Garg
Journal:  Curr Cardiol Rep       Date:  2014       Impact factor: 2.931

7.  Inflammatory regulation of valvular remodeling: the good(?), the bad, and the ugly.

Authors:  Gretchen J Mahler; Jonathan T Butcher
Journal:  Int J Inflam       Date:  2011-07-18

8.  De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.

Authors:  James R Priest; Kazutoyo Osoegawa; Nebil Mohammed; Vivek Nanda; Ramendra Kundu; Kathleen Schultz; Edward J Lammer; Santhosh Girirajan; Todd Scheetz; Daryl Waggott; Francois Haddad; Sushma Reddy; Daniel Bernstein; Trudy Burns; Jeffrey D Steimle; Xinan H Yang; Ivan P Moskowitz; Matthew Hurles; Richard P Lifton; Debbie Nickerson; Michael Bamshad; Evan E Eichler; Seema Mital; Val Sheffield; Thomas Quertermous; Bruce D Gelb; Michael Portman; Euan A Ashley
Journal:  PLoS Genet       Date:  2016-04-08       Impact factor: 5.917

9.  Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation.

Authors:  Evelise Brizola; Maria Gnoli; Morena Tremosini; Paolo Nucci; Sara Bargiacchi; Andrea La Barbera; Sabrina Giglio; Luca Sangiorgi
Journal:  Mol Genet Genomic Med       Date:  2020-06-17       Impact factor: 2.183

10.  Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment.

Authors:  Li Huang; Chonglin Chen; Zhirong Wang; Limei Sun; Songshan Li; Ting Zhang; Xiaoling Luo; Xiaoyan Ding
Journal:  Genes (Basel)       Date:  2020-08-03       Impact factor: 4.096

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