Literature DB >> 18209361

Methylmalonic acidemia with renal involvement: a case report and review of literature.

K V Srinivas1, M A Want, O S Freigoun, N Balakrishna.   

Abstract

Methylmalonic acidemia (MMA) is an inborn error of metabolism that results in the accumulation in blood, and increased excretion in the urine of, methylmalonic acid. It may present either as an acute, often fatal, condition in infancy, or in a more chronic intermittent form in older children. Organ involvement including kidneys has been described. We report here the presentation and management of a ten-year-old boy who had MMA and chronic renal failure.

Entities:  

Year:  2001        PMID: 18209361

Source DB:  PubMed          Journal:  Saudi J Kidney Dis Transpl        ISSN: 1319-2442


  3 in total

1.  Increased susceptibility of brain acetylcholinesterase activity to methylmalonate in young rats with renal failure.

Authors:  André C Affonso; Daniele G Machado; Fernanda Malgarin; Daiane B Fraga; Fernando Ghedim; Alexandra Zugno; Emílio L Streck; Patrícia F Schuck; Gustavo C Ferreira
Journal:  Metab Brain Dis       Date:  2013-03-09       Impact factor: 3.584

2.  Methylmalonic acid administration induces DNA damage in rat brain and kidney.

Authors:  Vanessa M Andrade; Hugo S Dal Pont; Daniela D Leffa; Adriani P Damiani; Giselli Scaini; Giana Hainzenreder; Emilio L Streck; Gustavo C Ferreira; Patrícia F Schuck
Journal:  Mol Cell Biochem       Date:  2014-02-15       Impact factor: 3.396

3.  Methylmalonic acidemia mimicking diabetic ketoacidosis and septic shock in infants.

Authors:  Navdeep Saini; Ashwini Malhotra; Sanjay Chhabra; Sunny Chhabra
Journal:  Indian J Crit Care Med       Date:  2015-03
  3 in total

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