Literature DB >> 14625237

Infantile refsum disease: case report.

Vaishali Choksi1, Ellen Hoeffner, Ercan Karaarslan, Cengiz Yalcinkaya, Sinan Cakirer.   

Abstract

Infantile Refsum disease is a rare inborn error of phytanic acid metabolism. It is inherited in an autosomal recessive manner and frequently causes signs and symptoms in the neonate period. The only source of phytanic acid in humans is exogenous, from diet. We report the MR imaging findings in two cases of infantile Refsum disease and note the MR imaging changes that occurred over time because of further progression of the disease. The initial diagnosis in both patients was made on basis of history, clinical findings, and biochemical studies.

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Year:  2003        PMID: 14625237      PMCID: PMC8148918     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  7 in total

1.  Refsum's disease in an Arabian family.

Authors:  E Fertl; D Földy; K Vass; E Auff; C Vass; B Molzer; H Bernheimer
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-04       Impact factor: 10.154

Review 2.  Refsum's disease.

Authors:  A J Wills; N J Manning; M M Reilly
Journal:  QJM       Date:  2001-08

3.  Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's disease.

Authors:  G A Jansen; R J Wanders; P A Watkins; S J Mihalik
Journal:  N Engl J Med       Date:  1997-07-10       Impact factor: 91.245

4.  MR findings in infantile Refsum disease: case report of two family members.

Authors:  J Dubois; G Sebag; M Argyropoulou; F Brunelle
Journal:  AJNR Am J Neuroradiol       Date:  1991 Nov-Dec       Impact factor: 3.825

5.  Infantile Refsum disease.

Authors:  S Naidu; H Moser
Journal:  AJNR Am J Neuroradiol       Date:  1991 Nov-Dec       Impact factor: 3.825

6.  Skeletal abnormalities in Refsum's disease (heredopathia atactica polyneuritiformis).

Authors:  G R Plant; D M Hansell; F B Gibberd; M C Sidey
Journal:  Br J Radiol       Date:  1990-07       Impact factor: 3.039

7.  Infantile Refsum's disease: a generalized peroxisomal disorder. Case report with postmortem examination.

Authors:  A Torvik; S Torp; B F Kase; J Ek; O Skjeldal; O Stokke
Journal:  J Neurol Sci       Date:  1988-05       Impact factor: 3.181

  7 in total
  6 in total

Review 1.  Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI.

Authors:  L Vedolin; G Gonzalez; C F Souza; C Lourenço; A J Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2012-05-17       Impact factor: 3.825

2.  The dentate nucleus in children: normal development and patterns of disease.

Authors:  Aoife McErlean; Khaled Abdalla; Veronica Donoghue; Stephanie Ryan
Journal:  Pediatr Radiol       Date:  2010-01-28

Review 3.  Characterization of Severity in Zellweger Spectrum Disorder by Clinical Findings: A Scoping Review, Meta-Analysis and Medical Chart Review.

Authors:  Mousumi Bose; Christine Yergeau; Yasmin D'Souza; David D Cuthbertson; Melisa J Lopez; Alyssa K Smolen; Nancy E Braverman
Journal:  Cells       Date:  2022-06-10       Impact factor: 7.666

4.  Infantile Refsum disease: serial evaluation with MRI.

Authors:  Sinan Cakirer; Mahmut R Savas
Journal:  Pediatr Radiol       Date:  2004-10-06

Review 5.  In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.

Authors:  Erica B Sherry; Phil Lee; In-Young Choi
Journal:  Neurochem Res       Date:  2015-11-26       Impact factor: 3.996

6.  Zellweger spectrum disorder: A cross-sectional study of symptom prevalence using input from family caregivers.

Authors:  Mousumi Bose; David D Cuthbertson; Marsha A Fraser; Jean-Baptiste Roullet; K Michael Gibson; Dana R Schules; Kelly M Gawron; Melissa B Gamble; Kathryn M Sacra; Melisa J Lopez; William B Rizzo
Journal:  Mol Genet Metab Rep       Date:  2020-12-10
  6 in total

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