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. 1977 Oct;52(10):796–798. doi: 10.1136/adc.52.10.796

Diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. 3 cases of 'DIDMOAD' syndrome.

J E Richardson, W Hamilton
PMCID: PMC1544785  PMID: 931428

Abstract

Three children with diabetes insipidus, diabetes mellitus, optic atrophy, and high-tone deafness were shown to lack vasopressin, indicative of degeneration of the cells of the hypothalamic supraoptic nuclei. The syndrome being due to a single gene defect, inherited as an autosomal recessive, is therefore likely to be the result of an inborn error of metabolism with variable periods of latency in those affected.

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Selected References

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

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