Literature DB >> 30210725

The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness.

Josef Finsterer1, Marlies Frank2.   

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.

Entities:  

Keywords:  DNA, Mitochondrial; Diabetes Mellitus; Epilepsy; Hypoacusis; Hypogonadism; Mitochondrial Diseases

Year:  2018        PMID: 30210725      PMCID: PMC6131922          DOI: 10.5001/omj.2018.80

Source DB:  PubMed          Journal:  Oman Med J        ISSN: 1999-768X


  27 in total

1.  Pearls & oy-sters: maternally inherited diabetes and deafness presenting with ptosis and macular pattern dystrophy.

Authors:  Olufunmilola Ogun; Claire Sheldon; Jason J S Barton
Journal:  Neurology       Date:  2012-08-07       Impact factor: 9.910

2.  Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA.

Authors:  K Tanaka; Y Takada; T Matsunaka; S Yuyama; S Fujino; M Maguchi; S Yamashita; I Yuba
Journal:  Intern Med       Date:  2000-03       Impact factor: 1.271

3.  Retinal branch vein occlusion associated with macular dystrophy, maternally inherited diabetes, and deafness.

Authors:  E Souied; B Mashhour; X Morel; Y Cohen; J P Bonnefond; A Munnich; D Chauvaud; G Renard; J Kaplan
Journal:  Ophthalmic Genet       Date:  1997-09       Impact factor: 1.803

4.  Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.

Authors:  P Massin; D Dubois-Laforgue; T Meas; M Laloi-Michelin; H Gin; B Bauduceau; C Bellanné-Chantelot; E Bertin; J-F Blickle; B Bouhanick; J Cahen-Varsaux; S Casanova; G Charpentier; P Chedin; O Dupuy; A Grimaldi; B Guerci; E Kaloustian; A Lecleire-Collet; F Lorenzini; A Murat; H Narbonne; F Olivier; V Paquis-Flucklinger; M Virally; M Vincenot; B Vialettes; J Timsit; P J Guillausseau
Journal:  Diabetologia       Date:  2008-06-26       Impact factor: 10.122

5.  A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.

Authors:  Najla Mezghani; Mouna Mnif; Emna Mkaouar-Rebai; Nozha Kallel; Nadia Charfi; Mohamed Abid; Faiza Fakhfakh
Journal:  Biochem Biophys Res Commun       Date:  2013-01-26       Impact factor: 3.575

6.  Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.

Authors:  Olga Azevedo; Laura Vilarinho; Filipa Almeida; Francisco Ferreira; Joana Guardado; Mariana Ferreira; António Lourenço; Rosa Medeiros; João Almeida
Journal:  Cardiology       Date:  2009-10-27       Impact factor: 1.869

7.  Maternally inherited diabetes and deafness (MIDD): diagnosis and management.

Authors:  Aye Naing; Manohar Kenchaiah; Binu Krishnan; Farheen Mir; Amanda Charnley; Catherine Egan; Gul Bano
Journal:  J Diabetes Complications       Date:  2014-03-12       Impact factor: 2.852

8.  Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

Authors:  Caren Bellmann; Magella M Neveu; Hendrik P N Scholl; Chris R Hogg; Pamela P Rath; Sharon Jenkins; Alan C Bird; Graham E Holder
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-07       Impact factor: 4.799

Review 9.  Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.

Authors:  J M van den Ouweland; H H Lemkes; K D Gerbitz; J A Maassen
Journal:  Muscle Nerve Suppl       Date:  1995

Review 10.  [Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation].

Authors:  Masako Mukai; Keizo Sugaya; Shiro Matsubara; Huaying Cai; Ichiro Yabe; Hidenao Sasaki; Imaharu Nakano
Journal:  Rinsho Shinkeigaku       Date:  2014
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  1 in total

Review 1.  The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.

Authors:  Mengge Yang; Lusi Xu; Chunmei Xu; Yuying Cui; Shan Jiang; Jianjun Dong; Lin Liao
Journal:  Front Endocrinol (Lausanne)       Date:  2021-11-25       Impact factor: 5.555

  1 in total

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