Literature DB >> 8723076

Revised diagnostic criteria for the Marfan syndrome.

A De Paepe1, R B Devereux, H C Dietz, R C Hennekam, R E Pyeritz.   

Abstract

In 1986, the diagnosis of the Marfan syndrome was codified on the basis of clinical criteria in the Berlin nosology [Beighton et al., 1988]. Over time, weaknesses have emerged in these criteria, a problem accentuated by the advent of molecular testing. In this paper, we propose a revision of diagnostic criteria for Marfan syndrome and related conditions. Most notable are: more stringent requirements for diagnosis of the Marfan syndrome in relatives of an unequivocally affected individual; skeletal involvement as a major criterion if at least 4 of 8 typical skeletal manifestations are present; potential contribution of molecular analysis to the diagnosis of Marfan syndrome; and delineation of initial criteria for diagnosis of other heritable conditions with partially overlapping phenotypes.

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Year:  1996        PMID: 8723076     DOI: 10.1002/(SICI)1096-8628(19960424)62:4<417::AID-AJMG15>3.0.CO;2-R

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


  284 in total

1.  Survival and complication free survival in Marfan's syndrome: implications of current guidelines.

Authors:  M Groenink; T A Lohuis; J G Tijssen; M S Naeff; R C Hennekam; E E van der Wall; B J Mulder
Journal:  Heart       Date:  1999-10       Impact factor: 5.994

Review 2.  Cardiovascular surgery for Marfan syndrome.

Authors:  T Treasure
Journal:  Heart       Date:  2000-12       Impact factor: 5.994

Review 3.  Diseases of the thoracic aorta.

Authors:  R Erbel
Journal:  Heart       Date:  2001-08       Impact factor: 5.994

Review 4.  Joint hypermobility and genetic collagen disorders: are they related?

Authors:  R Grahame
Journal:  Arch Dis Child       Date:  1999-02       Impact factor: 3.791

5.  Muscle fibrillin deficiency in Marfan's syndrome myopathy.

Authors:  W M H Behan; C Longman; R K H Petty; P Comeglio; A H Child; M Boxer; P Foskett; D G F Harriman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-05       Impact factor: 10.154

Review 6.  Management of Marfan syndrome.

Authors:  John C S Dean
Journal:  Heart       Date:  2002-07       Impact factor: 5.994

7.  Intraoperative conversion after surgical failure: an overlooked complication of aortic root replacement in Marfan patients?

Authors:  Irina V Volguina; Scott A LeMaire; Laura C Palmero; D Craig Miller; Joseph S Coselli
Journal:  Tex Heart Inst J       Date:  2011

8.  Can early aortic root surgery prevent further aortic dissection in Marfan syndrome?

Authors:  Hideyuki Shimizu; Hirofumi Kasahara; Atsushi Nemoto; Kentaro Yamabe; Toshihiko Ueda; Ryohei Yozu
Journal:  Interact Cardiovasc Thorac Surg       Date:  2011-11-30

9.  Medical treatment of crystalline lens dislocation into the anterior chamber in a patient with Marfan syndrome.

Authors:  Manuel Garza-Leon; Paola de la Parra-Colín
Journal:  Int Ophthalmol       Date:  2012-06-13       Impact factor: 2.031

10.  Genetic dissection of marfan syndrome and related connective tissue disorders: an update 2012.

Authors:  S Hoffjan
Journal:  Mol Syndromol       Date:  2012-06-12
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