Ehlers–Danlos Syndrome Type Arthrochalasia: A Systematic Review

Ehlers–Danlos syndrome type arthrochalasia (aEDS) is a rare genetic disease characterized by severe generalized joint hypermobility, bilateral congenital hip dislocation, skin hyperextensibility, muscle hypotonia, and mild dysmorphic features. It is an autosomal dominant connective tissue disease ca...

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Detalles Bibliográficos
Autores principales: Martín-Martín, Marta, Cortés-Martín, Jonathan, Tovar-Gálvez, Maria Isabel, Sánchez-García, Juan Carlos, Díaz-Rodríguez, Lourdes, Rodríguez-Blanque, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835098/
https://www.ncbi.nlm.nih.gov/pubmed/35162892
http://dx.doi.org/10.3390/ijerph19031870

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835098/
https://www.ncbi.nlm.nih.gov/pubmed/35162892
http://dx.doi.org/10.3390/ijerph19031870

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