Literature DB >> 3354620

Marfan syndrome: exclusion of genetic linkage to three major collagen genes.

C A Francomano1, E A Streeten, D A Meyers, R E Pyeritz.   

Abstract

The Marfan syndrome is an autosomal dominant connective tissue disorder with pleiotropic manifestations affecting skeletal, ocular and cardiovascular systems. Because the fibrillar collagens are major structural components of connective tissue, the hypothesis has long been set forth that the Marfan syndrome is a disorder of fibrillar collagen. We have investigated this hypothesis by performing linkage studies in 12 multiplex families with the Marfan syndrome, using restriction fragment length polymorphisms (RFLP's) associated with 3 genes encoding chains of fibrillar collagens. The data exclude linkage to all 3 candidate genes in 2 families and at least 1 of the candidates is excluded in 6 additional families. Each candidate was excluded in at least 3 families. In no case was strong evidence in favor of linkage of the Marfan syndrome to any of the 3 genes observed. These data speak against the hypothesis that mutations in one or more of these 3 fibrillar collagens cause the classic Marfan syndrome.

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Year:  1988        PMID: 3354620     DOI: 10.1002/ajmg.1320290233

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


  12 in total

1.  Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene.

Authors:  K Kainulainen; B Steinmann; F Collins; H C Dietz; C A Francomano; A Child; M W Kilpatrick; D J Brock; M Keston; R E Pyeritz
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

2.  Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.

Authors:  J de Groote; P A Farndon; M V Kilpatrick; A de Paepe; J W Oorthuys; N C Nevin; A H Child; F M Pope
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

3.  Linkage analysis in Marfan syndrome.

Authors:  R C Schwartz; S H Blanton; C A Hyde; T R Sottile; L Hudgins; M Sarfarazi; P Tsipouras
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

4.  Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family.

Authors:  C Boileau; G Jondeau; C Bonaiti; M Coulon; G Delorme; O Dubourg; J P Bourdarias; C Junien
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

5.  Marfan syndrome: light at the end of the tunnel?

Authors:  P Tsipouras
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

6.  An exclusion map of Marfan syndrome.

Authors:  S H Blanton; M Sarfarazi; H Eiberg; J de Groote; P A Farndon; M W Kilpatrick; A H Child; F M Pope; L Peltonen; C A Francomano
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

7.  Marfan syndrome: absence of type I or III collagen structural defects in 25 patients.

Authors:  V R Harley; D Chan; J G Rogers; W G Cole
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

8.  Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndrome.

Authors:  M Godfrey; S Olson; R G Burgio; A Martini; M Valli; G Cetta; H Hori; D W Hollister
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

9.  Marfan syndrome affecting four generations of a family without ocular involvement.

Authors:  A B Bridges; M Faed; M Boxer; W M Haining; T H Pringle; G P McNeill
Journal:  Postgrad Med J       Date:  1991-06       Impact factor: 2.401

10.  A substitution at a non-glycine position in the triple-helical domain of pro alpha 2(I) collagen chains present in an individual with a variant of the Marfan syndrome.

Authors:  C L Phillips; A W Shrago-Howe; S R Pinnell; R J Wenstrup
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

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