A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report
Abstract Kyphoscoliotic Ehlers–Danlos syndrome (kEDS) is a rare genetic disorder combining congenital hypotonia, congenital/early onset and progressive kyphoscoliosis, and generalized joint hypermobility. Vascular fragility is another characteristic of the disease rarely described. We report a sever...
Main Authors: | Malika Foy, Corinne Métay, Michael Frank, Nicolas Denarié, Salma Adham, Clarisse Billon, Anne Legrand, Xavier Jeunemaitre, Fabrice Gillas, Karen Gaudon, Philippe De Mazancourt, Ahmed Mekki, Robert Carlier, Karelle Benistan |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2023-02-01
|
Series: | Clinical Case Reports |
Subjects: | |
Online Access: | https://doi.org/10.1002/ccr3.6760 |
Similar Items
-
The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation
by: Xiaolin Ni, et al.
Published: (2020-10-01) -
A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
by: Rosaura Conti, et al.
Published: (2021-02-01) -
Classical Ehlers–Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of COL5A2
by: Malika Foy, et al.
Published: (2022-11-01) -
Genetic testing for vascular Ehlers-Danlos syndrome and other variants with fragility of the middle arteries
by: Rakhmanov Yeltay, et al.
Published: (2018-09-01) -
A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder
by: Malika Foy, et al.
Published: (2021-09-01)