| Literature DB >> 9686670 |
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.Entities:
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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