Literature DB >> 581217

Leukocyte docosahexaenoic acid in juvenile form of ceroid-lipofuscinosis.

R K Pullarkat, V K Patel, H Brockerhoff.   

Abstract

Leukocyte glycerolipid fatty acid compositions were determined in four patients of juvenile form of neuronal ceroid-lipofuscinosis (Battens disease), their parents and age-matched controls. A 54 to 93% reduction in docosahexaenoic acid (22:6, n-3) was noted in patient leukocytes. The parents also showed reduction in docosahexaenoic acid content, but to a lesser degree. The levels of linolenic family (n-6) polyunsaturated fatty acids were unchanged suggesting that the metabolic defect in this disease is specific to the linolenic family (n-3) of fatty acids.

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Year:  1978        PMID: 581217     DOI: 10.1055/s-0028-1085417

Source DB:  PubMed          Journal:  Neuropadiatrie        ISSN: 0028-3797


  3 in total

Review 1.  Metabolism and nervous system disease: a challenge for our times. Part II.

Authors:  E Roberts
Journal:  Metab Brain Dis       Date:  1986-06       Impact factor: 3.584

2.  Elevated levels of neutrophil 4-hydroxynonenal in canine neuronal ceroid-lipofuscinosis and human immortalized lymphocytes of NCL patients.

Authors:  A N Siakotos; F J van Kuijk; J A Tischfield
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Juvenile Batten's disease: an ophthalmological assessment of 26 patients.

Authors:  D J Spalton; D S Taylor; M D Sanders
Journal:  Br J Ophthalmol       Date:  1980-10       Impact factor: 4.638

  3 in total

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