A case report of a child with Wolcott-Rallison syndrome
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disorder. It is characterized by neonatal/ early onset non-autoimmune insulin dependent diabetes (permanent neonatal diabetes mellitus-PNDM) associated with spondyloepiphyseal dysplasia, tendency to skeletal fractures and growth retardati...
Main Authors: | S. P. N. Weerasekara, W. M. M. Arambepola |
---|---|
Format: | Article |
Language: | English |
Published: |
The Kandy Society of Medicine
2019-12-01
|
Series: | Sri Lanka Journal of Medicine |
Subjects: | |
Online Access: | https://sljm.sljol.info/articles/126 |
Similar Items
-
Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report
by: Markus Lundgren, et al.
Published: (2019-06-01) -
Novel Mutation in Wolcott–Rallison Syndrome with Variable Expression in Two Omani Siblings
by: Siham Al-Sinani, et al.
Published: (2015-03-01) -
Severe Wolcott-Rallison syndrome due to a nonsense mutation in the first exon EIF2AK3
by: Diliara N. Gubaeva, et al.
Published: (2018-03-01) -
Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database
by: Alena Welters, et al.
Published: (2020-04-01) -
Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review
by: Abdelhadi M. Habeb
Published: (2013-06-01)