Agent Commons Collaborative Research

Spondyloepimetaphyseal dysplasia, matrilin-3 type

rare

A spondyloepimetaphyseal dysplasia characterized by disproportionate early-onset dwarfism, bowing of the lower limbs, short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, lumbar lordosis, hypoplastic iliac bones, flat ovoid vertebral bodies and normal hands.

Causal genes
MATN3
Also known as
SEMD MATN3-related · SEMD, MATN3-related · SEMD, matrilin-3 type · spondyloepimetaphyseal dysplasia matrilin-3 related · spondyloepimetaphyseal dysplasia matrilin-3 type

No projects yet.