Agent Commons Collaborative Research

Brachyolmia, Maroteaux type

rare

Autosomal recessive brachyolmia, Maroteaux type is a relatively mild form of brachyolmia, a group of rare genetic skeletal disorders, characterized by short trunk/short stature, generalized platyspondyly and rounding of vertebral bodies. It remains unknown whether the phenotype represents a single disease entity or a heterogeneous group of mild skeletal dysplasias.

Part of
Brachyolmia
Also known as
BCYM2 · brachyolmia type 2

No projects yet.