Literature DB >> 16601890

The longest-surviving patient with classical maple syrup urine disease.

Carel le Roux1, Elaine Murphy, Maggie Lilburn, Philip J Lee.   

Abstract

The clinical problems, dietary management and biochemical monitoring over a 40-year period of the longest-surviving patient with maple syrup urine disease are described. Her case illustrates that a good outcome can be obtained with early diagnosis and institution of a diet restricted in branched-chain amino acids. Changes in dietary supplementation have benefited her in terms of nutrition and quality of life. Consistently high blood concentrations of branched-chain amino acids have not been associated with neuropsychometric decline.

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Year:  2006        PMID: 16601890     DOI: 10.1007/s10545-006-0204-4

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  7 in total

1.  DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

Authors:  R G WESTALL
Journal:  Arch Dis Child       Date:  1963-10       Impact factor: 3.791

2.  Developmental profile of patients with maple syrup urine disease.

Authors:  A Nord; W J van Doorninck; C Greene
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Corneal deepithelialization caused by acute deficiency of isoleucine during treatment of a patient with maple syrup urine disease.

Authors:  K Tornqvist; H Tornqvist
Journal:  Acta Ophthalmol Scand Suppl       Date:  1996

4.  Long term outcome of organic acidurias: survey of 105 French cases (1967-1983).

Authors:  R Rousson; P Guibaud
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

5.  Intellectual performance of children with maple syrup urine disease.

Authors:  C Hilliges; D Awiszus; U Wendel
Journal:  Eur J Pediatr       Date:  1993-02       Impact factor: 3.183

6.  Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia.

Authors:  S C Van Calcar; C O Harding; S R Davidson; L A Barness; J A Wolff
Journal:  Am J Med Genet       Date:  1992-11-15

7.  Ophthalmic findings in maple syrup urine disease.

Authors:  J P Burke; M O'Keefe; R Bowell; E R Naughten
Journal:  Metab Pediatr Syst Ophthalmol (1985)       Date:  1991
  7 in total
  1 in total

1.  Maple syrup urine disease in Cypriot families: identification of three novel mutations and biochemical characterization of the p.Thr211Met mutation in the E1alpha subunit.

Authors:  Theodoros Georgiou; Jacinta L Chuang; R Max Wynn; Goula Stylianidou; Mark Korson; David T Chuang; Anthi Drousiotou
Journal:  Genet Test Mol Biomarkers       Date:  2009-10
  1 in total

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