Spondyloepiphyseal dysplasia -- nephrotic syndrome: A very rare syndrome characterized by skeletal and immunity abnormalities. The immune defect leads to progressive kidney dysfunction which can ultimately cause death during the first decade. More detailed information about the symptoms, causes, and treatments of Spondyloepiphyseal dysplasia -- nephrotic syndrome is available below.
See full list of 26 symptoms of Spondyloepiphyseal dysplasia -- nephrotic syndrome
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Prognosis for Spondyloepiphyseal dysplasia -- nephrotic syndrome: death usually by 8 years of age
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Spondyloepiphyseal dysplasia -- nephrotic syndrome 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 -- nephrotic syndrome, or a subtype of Spondyloepiphyseal dysplasia -- nephrotic syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Spondyloepiphyseal dysplasia -- nephrotic syndrome as a "rare disease".
Source - Orphanet
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