ArticleOman medical journal2018
The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness.
Article in Oman medical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed.
- Diabetes control in m.3243 A > G carriers requires comprehensive consideration.Acta diabetologica · 2026Article
- Article
- The m.3243A>G variant affects not only islet, hair, or retinal ganglion cells, but all cells.GMS ophthalmology cases · 2025Article
- Mitochondrial diabetes plus phenotypes due to the m.3243A > G variant require correlation with heteroplasmy rates.Clinical case reports · 2024Article
- The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.Frontiers in endocrinology · 2021Review
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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