Spondyloepiphyseal dysplasia, congenita: A rare genetic bone growth disorder characterized by prenatal growth deficiency, myopia and short trunk. More detailed information about the symptoms, causes, and treatments of Spondyloepiphyseal dysplasia, congenita is available below.
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Spondyloepiphyseal dysplasia, congenita is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Spondyloepiphyseal dysplasia, congenita, or a subtype of Spondyloepiphyseal dysplasia, congenita,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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