Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1977 May;52(5):411–413. doi: 10.1136/adc.52.5.411

Congenital absence of islets of Langerhans.

J A Dodge, K M Laurence
PMCID: PMC1544555  PMID: 326201

Abstract

A small-for-dates male infant who developed acute metabolic acidosis shortly after birth had diabetes and died aged 40 hours. At necropsy there was an absence of any recognizable islets of Langerhans though lymphorecticular aggregates were found. This was the fourth child of healthy unrelated parents whose first child, also a male, died at 48 hours under similar circumstances. It is suggested that both boys had the same underlying pathology and this might be a previously undescribed recessive or x-linked inherited condition.

Full text

PDF
411

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. EMERY J. L., BURY H. P. INVOLUTIONARY CHANGES IN THE ISLETS OF LANGERHANS IN THE FOETUS AND NEWBORN. Biol Neonat. 1964;6:16–25. doi: 10.1159/000239884. [DOI] [PubMed] [Google Scholar]
  2. LECOMPTE P. M. Insulitis in early juvenile diabetes. AMA Arch Pathol. 1958 Oct;66(4):450–457. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES