Literature DB >> 10936976

Arylsulfatase A pseudodeficiency incidence in Turkey.

S Emre1, M Topçu, M Terzioğlu, Y Renda.   

Abstract

Pseudodeficiency (Pd) in arylsulfatase A (ASA) is a relatively frequent condition in healthy individuals. It produces a reduction in enzyme activity similar to that found in metachromatic leukodystrophy (MLD). A variable incidence of the Pd allele was found in different populations; it was 10-20 times higher than that of metachromatic leukodystrophy. Twelve of the 52 unrelated, healthy individuals were found to be heterozygous for the ASA Pd allele. In Turkey we estimated the incidence of the Pd allele as 11.5 percent. Out of 18 cases with MLD, one patient was found homozygous for the Pd allele and the other patient was found heterozygous.

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Year:  2000        PMID: 10936976

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  2 in total

1.  Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene.

Authors:  Alessandra Zanetti; Neslihan Onenli-Mungan; Nursel Elcioglu; Mehmet Nuri Ozbek; Deniz Kör; Elisabetta Lenzini; Maurizio Scarpa; Rosella Tomanin
Journal:  JIMD Rep       Date:  2013-11-16

2.  Late onset Aicardi-Goutières syndrome case report: a rare white matter disease mimicking as pseudo-enzyme deficiency.

Authors:  Melis Ulak Ozkan; Selahattin Katar; Edibe Pembegul Yildiz; Nur Aydinli; Mine Caliskan
Journal:  Acta Neurol Belg       Date:  2021-10-04       Impact factor: 2.396

  2 in total

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