Hachim, G. and Laarej, A. and Mahi, J. El and Abilkassem, R. and Hassani, A. and Agadr, A. (2022) A Case Report on Ehlers Danlos Syndrome. Asian Journal of Pediatric Research, 9 (4). pp. 1-5. ISSN 2582-2950
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Abstract
Ehlers-Danlos syndrome (EDS) is a group of hereditary collagen diseases characterized by joint hyperlaxity, skin hyperelasticity, and generalized tissue fragility. We present the case of an 8-year-old child with EDS in its arthrocalasic form type VII, according to the Villefranche classification, who was born to first-cousin parents. There is no curative treatment for EDS, but it is important to make an early diagnosis for optimal symptomatic management of patients and prevention of avoidable complications.
| Item Type: | Article |
|---|---|
| Subjects: | Opene Prints > Medical Science |
| Depositing User: | Managing Editor |
| Date Deposited: | 27 Jan 2023 05:56 |
| Last Modified: | 23 Mar 2024 04:22 |
| URI: | http://geographical.go2journals.com/id/eprint/1131 |
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