Literature DB >> 6517102

Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.

R I Kelley, H W Moser.   

Abstract

Serum pipecolic acid was measured in patients with neonatal adrenoleukodystrophy (NALD), sex-linked ALD, and the cerebrohepatorenal syndrome of Zellweger. Pipecolic acid was elevated, often markedly, in most of the patients with NALD but in none of those with X-linked ALD or adrenomyeloneuropathy, or in normal adults and children, or children with cirrhosis or other neurodegenerative disorders. The demonstration of elevated serum pipecolic acid in NALD adds to the previously recognized elevation of very-long-chain fatty acids (another Zellweger syndrome sign) and suggests that generalized peroxisomal dysfunction may be a characteristic of NALD as it appears to be of Zellweger syndrome, which diseases share some clinical characteristics. The nosologic significance of these findings is discussed.

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Year:  1984        PMID: 6517102     DOI: 10.1002/ajmg.1320190420

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  13 in total

Review 1.  Peroxisomal disorders: clinical characterization.

Authors:  L Monnens; H Heymans
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Authors:  B T Poll-The; J M Saudubray; H A Ogier; M Odièvre; J M Scotto; L Monnens; L C Govaerts; F Roels; A Cornelis; R B Schutgens
Journal:  Eur J Pediatr       Date:  1987-09       Impact factor: 3.183

Review 3.  Peroxisomal disorders: a newly recognised group of genetic diseases.

Authors:  R B Schutgens; H S Heymans; R J Wanders; H van den Bosch; J M Tager
Journal:  Eur J Pediatr       Date:  1986-02       Impact factor: 3.183

4.  Localization of pipecolic acid metabolism in rat liver peroxisomes: probable explanation for hyperpipecolataemia in Zellweger syndrome.

Authors:  J M Trijbels; L A Monnens; G Melis; M van den Broekvan Essen; M Bruckwilder
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

5.  Species variation in organellar location and activity of L-pipecolic acid oxidation in mammals.

Authors:  S J Mihalik; W J Rhead
Journal:  J Comp Physiol B       Date:  1991       Impact factor: 2.200

6.  Identification of L-amino acid/L-lysine alpha-amino oxidase in mouse brain.

Authors:  S N Murthy; M K Janardanasarma
Journal:  Mol Cell Biochem       Date:  1999-07       Impact factor: 3.396

7.  Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

Authors:  P B Lazarow; Y Fujiki; G M Small; P Watkins; H Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

8.  Transport of pipecolic acid in adult and developing mouse brain.

Authors:  J S Kim; E Giacobini
Journal:  Neurochem Res       Date:  1985-10       Impact factor: 3.996

9.  Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine.

Authors:  R A Roesel; J E Carroll; W B Rizzo; T van der Zalm; D A Hahn
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

10.  Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.

Authors:  W W Chen; P A Watkins; T Osumi; T Hashimoto; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1987-03       Impact factor: 11.205

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