Literature DB >> 17294289

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome with hypothyroidism and focal segmental glomerulosclerosis in a paediatric patient.

Keith K Lau1, Samuel P Yang, Maha N Haddad, Lavjay Butani, Sudesh P Makker.   

Abstract

Herein, we report on a paediatric patient with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) who was hospitalized for acute on chronic renal insufficiency, seizures and deterioration of the level of consciousness. She also had hypertension, hypothyroidism and nephrotic range proteinuria. Kidney biopsy revealed many sclerotic glomeruli and focal segmental glomerulosclerosis (FSGS). Glomerulopathy is rare in patients with MELAS, and FSGS has been reported only in a few patients. The histopathological features of the renal biopsy suggested that the aetiology of the FSGS may have been secondary to chronic renal injury rather than from a primary immunologic cause. Moreover, our case is unique in that, the coexistence of MELAS, hypothalamic hypothyroidism and FSGS has not been reported in the past. The purpose of this report is to increase the awareness of health-care professionals, especially in the fields of paediatrics, neurology, endocrinology and nephrology, regarding the manifestations and complications of MELAS.

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Year:  2007        PMID: 17294289     DOI: 10.1007/s11255-006-9172-8

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  23 in total

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Journal:  Clin Nephrol       Date:  1996-11       Impact factor: 0.975

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Authors:  S Ban; N Mori; K Saito; K Mizukami; T Suzuki; H Shiraishi
Journal:  Acta Pathol Jpn       Date:  1992-11
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  9 in total

1.  MELAS syndrome with rare manifestations misdiagnosed as vasculitis in the absence of lactic acidosis: A case report.

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Journal:  Ann Med Surg (Lond)       Date:  2022-08-27

2.  Renal manifestations of primary mitochondrial disorders.

Authors:  Josef Finsterer; Fulvio Alexandre Scorza
Journal:  Biomed Rep       Date:  2017-04-12

3.  An autopsy case of chronic progressive external ophthalmoplegia with renal insufficiency.

Authors:  Takashi Yuri; Yaeko Kondo; Keiko Kohno; Yen-Chang Lei; Seika Kanematsu; Maki Kuwata; Toshiji Iwasaka; Airo Tsubura
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4.  Mpv17 in mitochondria protects podocytes against mitochondrial dysfunction and apoptosis in vivo and in vitro.

Authors:  Gabriela Casalena; Stefanie Krick; Ilse Daehn; Liping Yu; Wenjun Ju; Shaolin Shi; Su-yi Tsai; Vivette D'Agati; Maja Lindenmeyer; Clemens D Cohen; Detlef Schlondorff; Erwin P Bottinger
Journal:  Am J Physiol Renal Physiol       Date:  2014-03-05

5.  Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome.

Authors:  Giorgina Barbara Piccoli; Laura Davico Bonino; Paola Campisi; Federica Neve Vigotti; Martina Ferraresi; Federica Fassio; Isabelle Brocheriou; Francesco Porpiglia; Gabriella Restagno
Journal:  BMC Nephrol       Date:  2012-02-21       Impact factor: 2.388

Review 6.  Monogenic Causes of Proteinuria in Children.

Authors:  Onur Cil; Farzana Perwad
Journal:  Front Med (Lausanne)       Date:  2018-03-12

7.  Klotho deficiency aggravates diabetes-induced podocyte injury due to DNA damage caused by mitochondrial dysfunction.

Authors:  Zhi Chen; Qing Zhou; Cong Liu; Yiping Zeng; Shaolong Yuan
Journal:  Int J Med Sci       Date:  2020-09-28       Impact factor: 3.738

Review 8.  Renal manifestations of genetic mitochondrial disease.

Authors:  John F O'Toole
Journal:  Int J Nephrol Renovasc Dis       Date:  2014-01-31

Review 9.  Endocrine disorders in mitochondrial disease.

Authors:  Andrew M Schaefer; Mark Walker; Douglass M Turnbull; Robert W Taylor
Journal:  Mol Cell Endocrinol       Date:  2013-06-13       Impact factor: 4.102

  9 in total

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