Literature DB >> 9810562

Hypertension in Leigh syndrome--a case report.

T Narita1, T Yamano, M Ohno, T Takano, R Ito, M Shimada.   

Abstract

A female patient, who was diagnosed with Leigh syndrome at 15 months of age, developed fulminating severe hypertension and died at 8 years of age. Hypertension has not been reported as an important clinical symptom in Leigh syndrome. Laboratory findings indicated that it was not associated with endocrinopathic diseases such as pheochromocytoma and aldosteronism, or renal diseases. Brain MRI scan showed symmetrical lesions in the basal ganglia and medulla oblongata including the nucleus tractus solitarius. This nucleus is known to play an important role in maintaining blood pressure. Since the medulla oblongata is a vulnerable site, potential development of hypertension should be taken into consideration when managing Leigh syndrome.

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Year:  1998        PMID: 9810562     DOI: 10.1055/s-2007-973572

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  3 in total

1.  Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia.

Authors:  Marcus Brecht; Malcolm Richardson; Ajay Taranath; Scott Grist; David Thorburn; Drago Bratkovic
Journal:  JIMD Rep       Date:  2015-02-15

2.  Leigh syndrome: serial MR imaging and clinical follow-up.

Authors:  J Arii; Y Tanabe
Journal:  AJNR Am J Neuroradiol       Date:  2000-09       Impact factor: 3.825

3.  MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.

Authors:  Laura Farina; Luisa Chiapparini; Graziella Uziel; Marianna Bugiani; Massimo Zeviani; Mario Savoiardo
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

  3 in total

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