The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness
Journal Title: Oman Medical Journal - Year 2018, Vol 33, Issue 5
Abstract
Maternally inherited diabetes and deafness (MIDD) is not only a disorder of the pancreas and ears but a multisystem mitochondrial disorder syndrome. Hypogonadism, however, has not been reported as a phenotypic feature of MIDD. We report a single case of a patient with MIDD which manifested clinically at 41 years old. In addition to diabetes and deafness, he manifested with seizures, ataxia, myopathy, and hypogonadism. We used established methods for the routine workup of this patient. MIDD is indeed a multisystem condition. A previously undescribed phenotypic feature of MIDD may be hypogonadism.
Authors and Affiliations
Josef Finsterer, Marlies Frank
Keywords
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- EP ID EP381018
- DOI 10.5001/omj.2018.80
- Views 97
- Downloads 0
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