A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes.
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DOI: 10.1016/j.jcjd.2017.06.009
Abstract: OBJECTIVE Wolcott-Rallison syndrome (WRS) is an extremely rare autosomal recessive condition, characterized by permanent neonatal diabetes mellitus (PNDM) associated with skeletal dysplasia, growth retardation and liver dysfunction. WRS is caused by biallelic mutations in the… read more here.
Keywords: wolcott rallison; clinical genetic; neonatal diabetes; rallison syndrome ... See more keywords
Clinical Experience from a Single Tertiary Care Center: Neonatal Diabetes Mellitus with Multiple Epiphyseal Dysplasia—Wolcott–Rallison's Syndrome
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DOI: 10.1055/s-0043-57005
Abstract: Abstract Wolcott–Rallison's syndrome (WRS) is a rare nonautoimmune autosomal recessive disorder characterized by neonatal diabetes mellitus, epiphyseal dysplasia, and growth retardation. This is the most common cause of diabetes mellitus in patients with consanguineous parents.… read more here.
Keywords: wolcott rallison; rallison syndrome; epiphyseal dysplasia; dysplasia ... See more keywords
Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database
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DOI: 10.1186/s13023-020-01359-y
Abstract: Background Wolcott-Rallison syndrome (WRS) is characterized by permanent early-onset diabetes, skeletal dysplasia and several additional features, e.g. recurrent liver failure. This is the first multicentre approach that focuses on diabetes management in WRS. We searched… read more here.
Keywords: diabetes management; wolcott rallison; german austrian; rallison syndrome ... See more keywords