Abstract
We describe a girl with Prader-Willi syndrome and membranoproliferative glomerulonephritis. She had a deletion at 15q11-13. The deletion may have made the child susceptible to renal disease.
MeSH terms
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Child
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Chromosome Deletion
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Chromosomes, Human, Pair 15 / physiology
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Female
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Glomerulonephritis, Membranoproliferative / genetics*
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Humans
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Prader-Willi Syndrome / complications
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Prader-Willi Syndrome / genetics*