Literature DB >> 1424198

Endocrine dysfunction in Kearns-Sayre syndrome.

J N Harvey1, D Barnett.   

Abstract

Kearns-Sayre syndrome (KSS) is a form of mitochondrial myopathy in which specific clinical features, namely progressive external ophthalmoplegia, pigmentary retinal degeneration and cardiac conduction defects, occur. KSS has also been associated with a variety of endocrine and metabolic disorders, in particular short stature, gonadal failure, diabetes mellitus, thyroid disease, hyperaldosteronism, hypomagnesaemia, and bone, tooth and calcification abnormalities. A case is described exhibiting all of these features. A survey of the literature was conducted to determine the prevalence of these conditions among reported cases. Cases with hypoparathyroidism were considered separately to see if they constituted a distinct subgroup with multiple endocrine dysfunction. Short stature was common, being documented in 38% of cases. Gonadal dysfunction before or after puberty was also common (20% of cases) and affected both sexes equally. Diabetes mellitus was recorded in 13% of cases, half of which required insulin. Thyroid disease, hyperaldosteronism and hypomagnesaemia were uncommon but were probably not looked for in many cases. Bone or tooth abnormalities and calcification of the basal ganglia were found both in those with and without hypoparathyroidism. While endocrine and metabolic dysfunction was found more commonly in those with hypoparathyroidism this is likely to be due to increased recognition rather than increased prevalence. No evidence of an autoimmune polyendocrine syndrome including hypoparathyroidism was found.

Entities:  

Mesh:

Year:  1992        PMID: 1424198     DOI: 10.1111/j.1365-2265.1992.tb02289.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  32 in total

1.  Obstetric anesthesia considerations in Kearns-Sayre syndrome: a case report.

Authors:  Ali S Faris; Qutaiba A Tawfic; Leo Jeyaraj
Journal:  Korean J Anesthesiol       Date:  2014-10-27

Review 2.  Hypoparathyroidism.

Authors:  John P Bilezikian
Journal:  J Clin Endocrinol Metab       Date:  2020-06-01       Impact factor: 5.958

3.  Primary adrenal insufficiency in a child with a mitochondrial DNA deletion.

Authors:  C Bruno; C Minetti; Y Tang; P J Magalhães; F M Santorelli; S Shanske; M Bado; G Cordone; R Gatti; S DiMauro
Journal:  J Inherit Metab Dis       Date:  1998-04       Impact factor: 4.982

4.  Large mitochondrial DNA deletion in an infant with addison disease.

Authors:  Gloria P Duran; A Martinez-Aguayo; H Poggi; M Lagos; D Gutierrez; P R Harris
Journal:  JIMD Rep       Date:  2011-09-22

Review 5.  Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELAS.

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

6.  Kearns-Sayre syndrome presenting as complete heart block.

Authors:  Sanjay Chawla; Jorida Coku; Thomas Forbes; Sujatha Kannan
Journal:  Pediatr Cardiol       Date:  2007-08-29       Impact factor: 1.655

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

Authors:  Conisha Mone Holloman; Lynne A Wolfe; William A Gahl; Cornelius F Boerkoel
Journal:  BMJ Case Rep       Date:  2013-02-18

Review 8.  Ophthalmic clues to the endocrine disorders.

Authors:  Z Liu; Y Chen; Z Lin; X Shi
Journal:  J Endocrinol Invest       Date:  2016-08-27       Impact factor: 4.256

9.  De Toni-Debré-Fanconi syndrome in a patient with Kearns-Sayre syndrome: a case report.

Authors:  Cristina Maria Mihai; Doina Catrinoiu; Marius Toringhibel; Ramona Mihaela Stoicescu; Anca Hancu
Journal:  J Med Case Rep       Date:  2009-11-03

10.  Combined occurrence of diabetes mellitus and retinitis pigmentosa.

Authors:  Afaf Al-Adsani; Fadl Abdel Gader
Journal:  Ann Saudi Med       Date:  2010 Jan-Feb       Impact factor: 1.526

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.