Literature DB >> 8403116

Anaesthetic implications of cystinosis.

J D Tobias1.   

Abstract

The author presents and discusses the anaesthetic care of a 12-yr-old boy with cystinosis. Cystinosis is a recessively inherited disorder of amino acid metabolism resulting in the abnormal intracellular accumulation of cystine. Anaesthetic care may be affected by variable end-organ involvement, most notably progressive renal deterioration beginning with the development of Fanconi syndrome and progressing to overt renal failure during the first decade of life. Additional organ system involvement may lead to cirrhosis with portal hypertension, diabetes mellitus, and hypothyroidism. Identification of the extent of end-organ involvement during the preoperative evaluation will help in the provision of safe anaesthetic care for such patients.

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Year:  1993        PMID: 8403116     DOI: 10.1007/BF03009734

Source DB:  PubMed          Journal:  Can J Anaesth        ISSN: 0832-610X            Impact factor:   5.063


  4 in total

1.  Diagnosis and treatment of renal tubular disorders in children.

Authors:  R A Donckerwolcke
Journal:  Pediatr Clin North Am       Date:  1982-08       Impact factor: 3.278

2.  Fanconi syndrome and anesthesia.

Authors:  M Joel; J K Rosales
Journal:  Anesthesiology       Date:  1981-10       Impact factor: 7.892

3.  Magnesium in the prevention of lethal arrhythmias in acute myocardial infarction.

Authors:  A S Abraham; D Rosenmann; M Kramer; J Balkin; M M Zion; H Farbstien; U Eylath
Journal:  Arch Intern Med       Date:  1987-04

4.  Cystinosis presenting with features suggesting Bartter syndrome. Case report and literature review.

Authors:  M P Whyte; S Shaheb; H W Schnaper
Journal:  Clin Pediatr (Phila)       Date:  1985-08       Impact factor: 1.168

  4 in total

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