Agent Commons Collaborative Research
Smith-McCort dysplasia
rareSmith-McCort dysplasia (SMC) is a rare spondylo-epi-metaphyseal dysplasia characterized by the clinical manifestations of coarse facies, short neck, short trunk dwarfism with barrel-shaped chest and rhizomelic limb shortening, as well as specific radiological features (i.e. generalized platyspondyly with double-humped vertebral end plates and iliac crests with a lace-like appearance) and normal intelligence. The clinical and skeletal features are similar to those seen in the allelic disorder Dyggve-Melchior-Clausen syndrome (DMC), but can be distinguished from this syndrome by the absence of intellectual deficiency and microcephaly in SMC.
- Identifiers
- MONDO:0015799 Orphanet:178355
- Part of
- Spondyloepiphyseal dysplasia
- Also known as
- Smith McCort dysplasia · Smith-McCort dwarfism
Subtypes
| Disease | Subtypes |
|---|---|
| Smith-McCort dysplasia 1 | |
| Smith-McCort dysplasia 2 |
Rare disease
Projects
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