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
|Instance of||rare disease,|
developmental defect during embryogenesis
|Subclass of||autosomal recessive disease,|
developmental anomaly of metabolic origin,
rare diabetes mellitus,
rare genetic diabetes mellitus
Media in category "Wolcott–Rallison syndrome"
This category contains only the following file.
- Walcott-Rallison Syndrome.png 900 × 1,183; 658 KB