Wolcott-Rallison syndrome anglès (Q8029730)

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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 anglès
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    Wolcott-Rallison syndrome
    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
    • Epiphyseal dysplasia multiple with early-onset diabetes mellitus
    • WRS
    • Med-Iddm Syndrome
    • Early-onset diabetes mellitus with multiple epiphyseal dysplasia
    • Iddm-Med Syndrome
    • Wolcott-Rallison Syndrome
    • Wolcott Rallison syndrome
    • EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS

    Declaracions

    Wolcott–Rallison syndrome
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