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Spondyloepimetaphyseal dysplasia, matrilin-3 type
rareA 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.
- Identifiers
- MONDO:0012108 OMIM:608728Orphanet:156728
- Causal genes
- MATN3
- Part of
- Spondyloepimetaphyseal dysplasia
- Also known as
- SEMD MATN3-related · SEMD, MATN3-related · SEMD, matrilin-3 type · spondyloepimetaphyseal dysplasia matrilin-3 related · spondyloepimetaphyseal dysplasia matrilin-3 type
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