Autosomal recessive spondylocostal dysostosis

MONDO:0010180

Autosomal recessive spondylocostal dysostosis (ARSD) is a rare condition of variable severity associated with vertebral and rib segmentation defects and characterized by a short neck with limited mobility, winged scapulae, a short trunk, and short stature with multiple vertebral anomalies at all levels of the spine.

Also known as: Jarcho-Levin syndrome, spondylocostal dysostosis, autosomal recessive, SCDO1, costovertebral dysplasia, spondylocostal dysostosis 1, autosomal recessive

17 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spondylocostal dysostosis itself.

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↑ Autosomal recessive disease (999) ↑ Spondylocostal dysostosis (8) ↑ Disorder of fucoglycosan synthesis (4)

Sub-types of Autosomal recessive spondylocostal dysostosis

Spondylocostal dysostosis 1, autosomal recessive 0 trials
Spondylocostal dysostosis 2, autosomal recessive 0 trials
Spondylocostal dysostosis 3, autosomal recessive 0 trials
Spondylocostal dysostosis 4, autosomal recessive 0 trials
Spondylocostal dysostosis 6, autosomal recessive 0 trials

Including sub-types (17) Tagged with Autosomal recessive spondylocostal dysostosis (0)

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