TY  - JOUR
AU  - Martín-Martín, Marta
AU  - Cortés-Martín, Jonathan
AU  - Tovar-Gálvez, Maria Isabel
AU  - Sánchez-García, Juan Carlos
AU  - Díaz-Rodríguez, Lourdes
AU  - Rodríguez-Blanque, Raquel
PY  - 2022
DO  - 10.3390/ijerph19031870
UR  - http://hdl.handle.net/10668/21029
T2  - International journal of environmental research and public health
AB  - 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...
LA  - en
KW  - EDS arthrochalasia
KW  - Ehlers–Danlos syndrome (EDS)
KW  - congenital anomaly
KW  - connective tissue
KW  - hypermobility
KW  - rare disease
KW  - systematic review
KW  - Collagen
KW  - Ehlers-Danlos Syndrome
KW  - Humans
KW  - Joint Instability
KW  - Quality of Life
KW  - Skin Abnormalities
TI  - Ehlers-Danlos Syndrome Type Arthrochalasia: A Systematic Review.
TY  - research article
VL  - 19
ER  -