Literature DB >> 23263430

Wolcott-Rallison syndrome.

A Juneja1, A Sultan, S Bhatnagar.   

Abstract

Multiple epiphyseal dysplasia with early-onset diabetes mellitus (also known as Wolcott-Rallison syndrome) is a rare autosomal recessive disorder that manifests itself in early infancy with symptoms of diabetes mellitus. Short stature and walking difficulties become evident in the 2 nd year of life when the child starts to walk. These skeletal changes are progressive with age. There is usually a short trunk, excessive lordosis, a short and broad chest, and genu valgum. This report presents a case of Wolcott-Rallison syndrome in a 10 year old child.

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Year:  2012        PMID: 23263430     DOI: 10.4103/0970-4388.105019

Source DB:  PubMed          Journal:  J Indian Soc Pedod Prev Dent        ISSN: 0970-4388


  1 in total

1.  Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation.

Authors:  Fatih Gürbüz; Bilgin Yüksel; Ali Kemal Topaloğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-06-04
  1 in total

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