Literature DB >> 3788757

The Marfan syndrome.

R E Pyeritz.   

Abstract

Although the prognosis for a person with the Marfan syndrome is much more favorable than it was a decade ago, this remains a serious and burdensome condition. Early diagnosis is essential and is based on characteristic abnormalities of the musculoskeletal, ocular and cardiovascular systems and a positive family history for the syndrome. Management focuses on recognizing abnormalities and altering the natural history of each clinical manifestation at as young an age as possible. The family physician must be current with therapy and counseling.

Entities:  

Mesh:

Year:  1986        PMID: 3788757

Source DB:  PubMed          Journal:  Am Fam Physician        ISSN: 0002-838X            Impact factor:   3.292


  5 in total

1.  Dural ectasia is a common feature of the Marfan syndrome.

Authors:  R E Pyeritz; E K Fishman; B A Bernhardt; S S Siegelman
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

2.  Ascertainment and severity of Marfan syndrome in a Scottish population.

Authors:  J R Gray; A B Bridges; M J Faed; T Pringle; P Baines; J Dean; M Boxer
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

3.  A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression.

Authors:  Bruno L Lima; Enrico J C Santos; Gustavo R Fernandes; Christian Merkel; Marco R B Mello; Juliana P A Gomes; Marina Soukoyan; Alexandre Kerkis; Silvia M G Massironi; José A Visintin; Lygia V Pereira
Journal:  PLoS One       Date:  2010-11-30       Impact factor: 3.240

4.  Trends and characteristics of congenital ectopia lentis in China.

Authors:  Guang-Ming Jin; Min Fan; Qian-Zhong Cao; Jun-Xiong Lin; Yi-Chi Zhang; Jian-Qiang Lin; Yi-Yao Wang; Charlotte-Aimee Young; Dan-Ying Zheng
Journal:  Int J Ophthalmol       Date:  2018-09-18       Impact factor: 1.779

5.  Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.

Authors:  K Kainulainen; A Savolainen; A Palotie; I Kaitila; J Rosenbloom; L Peltonen
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132

  5 in total

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