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Article

Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.

Ophthalmic genetics - 1 Jun 2021

Oishi Noriko, Kubota Daiki, Nakamoto Kenji, Takeda Yukito, Hayashi Mika, Gocho Kiyoko, Yamaki Kunihiko, Igarashi Tsutomu, Takahashi Hiroshi, Kameya Shuhei

Abstract excerpt

Purpose: Maternally inherited diabetes and deafness (MIDD) is caused by a heteroplasmic m.3243A>G mutation in the mitochondrial DNA. The main ocular feature in MIDD is macular dystrophy. The purpose of this study was to identify the phenotypical characteristics of a patient with MIDD by multimodal high-resolution imaging analyses.Methods: A detailed history and ophthalmic examination were performed on a...

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Identifiers

PMID: 33541179
DOI: 10.1080/13816810.2021.1881978

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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