Literature DB >> 6463246

Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic features.

D J Sartoris, L Luzzatti, D D Weaver, J D Macfarlane, D W Hollister, B R Parker.   

Abstract

The authors describe 7 male patients from two unrelated families who presented with what appears to be a heretofore undiagnosed X-linked variant of Ehlers-Danlos syndrome. Unlike the eight previously reported types, this variant is manifested by specific skeletal abnormalities, including occipital exostoses, widening and bowing of multiple long bones at tendinous and ligamentous insertion sites, and deformed clavicles. Major clinical complications include genitourinary problems, chronic diarrhea with malabsorption, and/or syncopal episodes. Laboratory tests suggest that this variant may represent the true lysyl-oxidase-deficient form of Ehlers-Danlos syndrome.

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Year:  1984        PMID: 6463246     DOI: 10.1148/radiology.152.3.6463246

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  12 in total

1.  Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree.

Authors:  A C Nicholls; A De Paepe; P Narcisi; R Dalgleish; F De Keyser; M Matton; F M Pope
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

2.  The Ehlers-Danlos syndrome, type IV, with an unusual combination of organ malformations.

Authors:  T Kahn; M Reiser; J Gmeinwieser; A Heuck
Journal:  Cardiovasc Intervent Radiol       Date:  1988-10       Impact factor: 2.740

3.  Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large family.

Authors:  B P Sokolov; A N Prytkov; G Tromp; R G Knowlton; D J Prockop
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

4.  Occipital horn syndrome in a woman: skeletal radiological findings.

Authors:  Alberto Bazzocchi; Rayka Femia; Paola Feraco; Giuseppe Battista; Romeo Canini; Giuseppe Guglielmi
Journal:  Skeletal Radiol       Date:  2011-05-08       Impact factor: 2.199

5.  Occipital horn syndrome. Additional radiographic findings in two new cases.

Authors:  T E Herman; W H McAlister; A Boniface; M P Whyte
Journal:  Pediatr Radiol       Date:  1992

6.  Variability in clinical expression of Menkes syndrome.

Authors:  A M Gerdes; T Tønnesen; E Pergament; C Sander; K E Baerlocher; R Wartha; F Güttler; N Horn
Journal:  Eur J Pediatr       Date:  1988-11       Impact factor: 3.183

7.  Huge bladder diverticula associated with Ehlers-Danlos syndrome.

Authors:  P M Cuckow; R J Blackhall; P D Mouriquand
Journal:  J R Soc Med       Date:  1994-05       Impact factor: 18.000

Review 8.  Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.

Authors:  Dawn Mikelonis; Cheryl L Jorcyk; Ken Tawara; Julia Thom Oxford
Journal:  Orphanet J Rare Dis       Date:  2014-03-12       Impact factor: 4.123

Review 9.  Menkes disease: what a multidisciplinary approach can do.

Authors:  Rahul Ojha; Asuri N Prasad
Journal:  J Multidiscip Healthc       Date:  2016-08-17

10.  A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype.

Authors:  Maria Teresa Bonati; Federico Verde; Uros Hladnik; Paola Cattelan; Luca Campana; Chiara Castronovo; Nicola Ticozzi; Luca Maderna; Claudia Colombrita; Sergio Papa; Paolo Banfi; Vincenzo Silani
Journal:  Mol Genet Metab Rep       Date:  2017-07-21
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