Literature DB >> 3284750

Diabetes mellitus in Kearns-Sayre syndrome.

Y Tanabe1, S Miyamoto, Y Kinoshita, K Yamada, N Sasaki, E Makino, H Nakajima.   

Abstract

A 20-year-old woman with Kearns-Sayre syndrome (KSS) suddenly experienced two episodes of diabetic coma. She was studied to determine whether diabetes mellitus (DM) resulted from insulin resistance or from an insulin secretion abnormality, using the euglycemic glucose clamp technique and the glucagon tolerance test. She had a deficiency of insulin secretion from beta cells. It is important to recognize in practice the onset of DM in patients with mitochondrial myopathy. We would suggest that a genetic linkage or mitochondrial dysfunction may be responsible for the association of both disease states.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3284750     DOI: 10.1159/000116225

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  9 in total

Review 1.  Does the mitochondrial DNA play a role in the pathogenesis of diabetes?

Authors:  K D Gerbitz
Journal:  Diabetologia       Date:  1992-12       Impact factor: 10.122

Review 2.  Maternally inherited diabetes and deafness: a new diabetes subtype.

Authors:  J A Maassen; T Kadowaki
Journal:  Diabetologia       Date:  1996-04       Impact factor: 10.122

Review 3.  The genes influencing the susceptibility to IDDM in humans.

Authors:  S Faas; M Trucco
Journal:  J Endocrinol Invest       Date:  1994 Jul-Aug       Impact factor: 4.256

4.  Pearson's marrow/pancreas syndrome: a histological and genetic study.

Authors:  Y Morikawa; N Matsuura; K Kakudo; R Higuchi; M Koike; Y Kobayashi
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

Review 5.  The development of mitochondrial medicine.

Authors:  R Luft
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

6.  Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia.

Authors:  A Quade; S Zierz; D Klingmüller
Journal:  Clin Investig       Date:  1992-05

7.  Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus.

Authors:  S Zierz; G Jahns; F Jerusalem
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

8.  Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspects.

Authors:  M S Damian; H Reichmann; H J Schütz; W Dorndorf; W Schachenmayr
Journal:  J Neurol       Date:  1991-04       Impact factor: 4.849

9.  Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Authors:  S Suzuki; Y Hinokio; S Hirai; M Onoda; M Matsumoto; M Ohtomo; H Kawasaki; Y Satoh; H Akai; K Abe
Journal:  Diabetologia       Date:  1994-08       Impact factor: 10.122

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.