Literature DB >> 1600349

Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia.

A Quade1, S Zierz, D Klingmüller.   

Abstract

Endocrine functions were examined in 21 patients with mitochondrial myopathies presenting with chronic progressive external ophthalmoplegia and other additional neurological and multisystemic symptoms. Ten patients had the features of the Kearns-Sayre syndrome. Deletions of the mitochondrial DNA were found in 4 out of 5 patients examined. Fourteen patients, including 3 with deletions of the mitochondrial DNA, had various and often multiple endocrine abnormalities: 6 patients were of short stature, 3 had irregular menstrual cycles, 3 had undersized testicles, 5 showed an insufficient rise of growth hormone following the administration of growth-hormone-releasing hormone, 4 showed an insufficient rise in FSH after administration of gonadotropin-releasing hormone, 5 had manifest diabetes mellitus, 3 showed an impaired glucose tolerance, and 2 patients had subnormal serum levels of parathormone in combination with hypocalcaemia. One patient additionally had Klinefelter's syndrome with a kariotype 47, XXY and increased levels of FSH and LH, subnormal levels of testosterone and subnormal testicular volume. The occurrence of endocrine defects correlated with the duration of disease. The data demonstrate that endocrine abnormalities are frequently associated with mitochondrial myopathy, indicating that this multisystemic disease also involves various endocrine tissues.

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Year:  1992        PMID: 1600349     DOI: 10.1007/bf00235520

Source DB:  PubMed          Journal:  Clin Investig        ISSN: 0941-0198


  23 in total

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Journal:  N Engl J Med       Date:  1987-08-20       Impact factor: 91.245

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  12 in total

1.  Delayed motherhood increases the probability of sons to be infertile.

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Journal:  J Assist Reprod Genet       Date:  2001-12       Impact factor: 3.412

2.  Normal pituitary function in a Japanese patient with Barth syndrome.

Authors:  Yuriko Katsushima; Ikuma Fujiwara; Osamu Sakamoto; Toshihiro Ohura; Shigeaki Miyabayashi; Akira Ohnuma; Seiji Yamaguchi; Kazuie Iinuma
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3.  Primary adrenal insufficiency in a child with a mitochondrial DNA deletion.

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Review 4.  Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELAS.

Authors:  Bruce H Cohen
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

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Review 6.  Mitochondrial disease and endocrine dysfunction.

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7.  Kearns-Sayre syndrome presenting as isolated growth failure.

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Review 8.  Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.

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Journal:  Genet Med       Date:  2017-07-27       Impact factor: 8.822

9.  A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment.

Authors:  Monika Obara-Moszynska; Jaroslaw Maceluch; Waldemar Bobkowski; Artur Baszko; Oskar Jaremba; Maciej R Krawczynski; Marek Niedziela
Journal:  BMC Pediatr       Date:  2013-02-20       Impact factor: 2.125

Review 10.  Endocrine manifestations related to inherited metabolic diseases in adults.

Authors:  Marie-Christine Vantyghem; Dries Dobbelaere; Karine Mention; Jean-Louis Wemeau; Jean-Marie Saudubray; Claire Douillard
Journal:  Orphanet J Rare Dis       Date:  2012-01-28       Impact factor: 4.123

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