Category:Wolcott–Rallison syndrome
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Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure | |||||
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Media in category "Wolcott–Rallison syndrome"
The following 5 files are in this category, out of 5 total.
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Walcott-Rallison Syndrome.png 900 × 1,183; 658 KB
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Wolcott-Rallison-Syndrom 21mM - WS CR seitlich - 001.jpg 278 × 1,094; 24 KB
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Wolcott-Rallison-Syndrom 2M - CR seitlich - 001.jpg 742 × 1,108; 65 KB
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Wolcott-Rallison-Syndrom 2M - OSG CR ap - 001.jpg 676 × 1,118; 48 KB
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Wolcott-Rallison-Syndrom 3M - Becken CR ap - 001.jpg 1,318 × 1,112; 88 KB