Literature DB >> 9686670

Ehlers-Danlos Syndrome Type VI (EDS VI): problems of diagnosis and management.

P Heim1, M Raghunath, L Meiss, U Heise, R Myllylä, A Kohlschütter, B Steinmann.   

Abstract

Ehlers-Danlos Syndrome Type VI (EDS VI) is a rare autosomal recessively inherited connective tissue disorder, which poses several problems of diagnosis and management. We report on a patient who developed severe kyphoscoliosis long before the diagnosis was reached. We conclude that early biochemical diagnosis and a timely operative procedure by extensive posterior instrumentation is the basis for successful management of this disorder.

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Year:  1998        PMID: 9686670     DOI: 10.1080/080352598750014184

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  3 in total

1.  Arterial fragility in kyphoscoliotic Ehlers-Danlos syndrome.

Authors:  Pierrick Henneton; Anne Legrand; Cecilia Giunta; Michael Frank
Journal:  BMJ Case Rep       Date:  2018-07-06

2.  Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl.

Authors:  Irene Brunk; Brigitte Stöver; Chrysanthy Ikonomidou; Jürgen Brinckmann; Luitgard M Neumann
Journal:  Eur J Pediatr       Date:  2004-02-11       Impact factor: 3.183

3.  Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome--an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13.

Authors:  Cecilia Giunta; Nursel H Elçioglu; Beate Albrecht; Georg Eich; Céline Chambaz; Andreas R Janecke; Heather Yeowell; MaryAnn Weis; David R Eyre; Marius Kraenzlin; Beat Steinmann
Journal:  Am J Hum Genet       Date:  2008-06       Impact factor: 11.025

  3 in total

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