Wolcott Rallison syndrome: a rare inherited diabetes mellitus.

Abstract

A 9-y-old boy was referred to authors' institute for the management of insulin dependent diabetes mellitus. He was the product of third degree consanguineous marriage and was delivered by full term vaginal delivery with a birth weight of 2.75 kg. At 3 mo of age, he had presented with diabetic ketoacidosis and was on insulin regimen. Patient had delayed milestones and short stature. On follow up, child developed limb deformity and was diagnosed to have skeletal dysplasia. At the age of 9 y, patient was diagnosed to have cirrhosis of liver. Genetic analysis revealed homozygous EIF2AK3 nonsense mutation. It confirmed the diagnosis of Wolcott-Rallison syndrome. Patient's mother was heterozygous for the same mutation.

• Authors: Shruti Khare, Manjunath Ramappa Goroshi, Sweta Budyal, Tushar Bandgar, Anurag Lila, Nalini Shah
• Journal: Indian journal of pediatrics (Indian J Pediatr) Vol. 81 Issue 11 Pg. 1225-7 (Nov 2014) ISSN: 0973-7693 [Electronic] India
• PMID: 24710710 (Publication Type: Case Reports, Journal Article)

Topics

• Child
• Consanguinity
• Diabetes Mellitus, Type 1 (diagnosis, genetics)
• Diagnosis, Differential
• Epiphyses (abnormalities)
• Humans
• India
• Male
• Osteochondrodysplasias (diagnosis, genetics)