Literature DB >> 9557891

Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

P Beighton1, A De Paepe, B Steinmann, P Tsipouras, R J Wenstrup.   

Abstract

Categorization of the Ehlers-Danlos syndromes began in the late 1960s and was formalized in the Berlin nosology. Over time, it became apparent that the diagnostic criteria established and published in 1988 did not discriminate adequately between the different types of Ehlers-Danlos syndromes or between Ehlers-Danlos syndromes and other phenotypically related conditions. In addition, elucidation of the molecular basis of several Ehlers-Danlos syndromes has added a new dimension to the characterization of this group of disorders. We propose a revision of the classification of the Ehlers-Danlos syndromes based primarily on the cause of each type. Major and minor diagnostic criteria have been defined for each type and complemented whenever possible with laboratory findings. This simplified classification will facilitate an accurate diagnosis of the Ehlers-Danlos syndromes and contribute to the delineation of phenotypically related disorders.

Mesh:

Year:  1998        PMID: 9557891     DOI: 10.1002/(sici)1096-8628(19980428)77:1<31::aid-ajmg8>3.0.co;2-o

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


  349 in total

1.  Null alleles of the COL5A1 gene of type V collagen are a cause of the classical forms of Ehlers-Danlos syndrome (types I and II).

Authors:  U Schwarze; M Atkinson; G G Hoffman; D S Greenspan; P H Byers
Journal:  Am J Hum Genet       Date:  2000-05-04       Impact factor: 11.025

Review 2.  The Ehlers-Danlos syndrome: on beyond collagens.

Authors:  J R Mao; J Bristow
Journal:  J Clin Invest       Date:  2001-05       Impact factor: 14.808

3.  Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis.

Authors:  Gabe Haller; Hannah Zabriskie; Shelby Spehar; Timothy Kuensting; Xavier Bledsoe; Ali Syed; Christina A Gurnett; Matthew B Dobbs
Journal:  J Pediatr Orthop B       Date:  2018-03       Impact factor: 1.041

4.  Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13.

Authors:  Nazneen Rahman; Melanie Dunstan; M Dawn Teare; Sandra Hanks; Jenny Douglas; Kim Coleman; William E Bottomly; Mary E Campbell; Britta Berglund; Magnus Nordenskjöld; Bengt Forssell; Nigel Burrows; Peter Lunt; Ian Young; Nigel Williams; Graham R Bignell; P Andrew Futreal; F Michael Pope
Journal:  Am J Hum Genet       Date:  2003-05-29       Impact factor: 11.025

5.  Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome.

Authors:  Manon C Zweers; Jim Bristow; Peter M Steijlen; Willow B Dean; Ben C Hamel; Marisol Otero; Martina Kucharekova; Jan B Boezeman; Joost Schalkwijk
Journal:  Am J Hum Genet       Date:  2003-07       Impact factor: 11.025

6.  Ehlers-Danlos syndrome hypermobility type: a possible unifying concept for various functional somatic syndromes.

Authors:  Marco Castori; Claudia Celletti; Filippo Camerota
Journal:  Rheumatol Int       Date:  2011-12-23       Impact factor: 2.631

Review 7.  Visceroptosis of the bowel in the hypermobility type of Ehlers-Danlos syndrome: presentation of a rare manifestation and review of the literature.

Authors:  Eyal Reinstein; Mark Pimentel; Mitchel Pariani; Stephen Nemec; Thomas Sokol; David L Rimoin
Journal:  Eur J Med Genet       Date:  2012-07-07       Impact factor: 2.708

8.  The haploinsufficient Col3a1 mouse as a model for vascular Ehlers-Danlos syndrome.

Authors:  T K Cooper; Q Zhong; M Krawczyk; H-J Tae; G A Müller; R Schubert; L A Myers; H C Dietz; M I Talan; W Briest
Journal:  Vet Pathol       Date:  2010-06-29       Impact factor: 2.221

9.  Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.

Authors:  Eyal Reinstein; Sophia Frentz; Tim Morgan; Sixto García-Miñaúr; Richard J Leventer; George McGillivray; Mitchel Pariani; Anthony van der Steen; Michael Pope; Muriel Holder-Espinasse; Richard Scott; Elizabeth M Thompson; Terry Robertson; Brian Coppin; Robert Siegel; Montserrat Bret Zurita; Jose I Rodríguez; Carmen Morales; Yuri Rodrigues; Joaquín Arcas; Anand Saggar; Margaret Horton; Elaine Zackai; John M Graham; David L Rimoin; Stephen P Robertson
Journal:  Eur J Hum Genet       Date:  2012-10-03       Impact factor: 4.246

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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