Dergiler / Turkish Journal of Pediatrics / 2000 / Cilt: 42 - Sayı: 2

Arylsulfatase a pseudodeficiency incidence in Turkey

Sayfa
115–117
Yayın Tarihi
2022-11-04
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Out of 18 cases with MLD, one patient was found homozygous for the Pd allele and the other patient was found heterozygous.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Pseudodeficiency (Pd) in arylsulfatase A (ASA) is a relatively frequent condition in healthy individuals.
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Temel Bulgular & Veri:A variable incidence of the Pd allele was found in different populations; it was 10-20 times higher than that of metachromatic leukodystrophy.
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Sonuç & Katkı:Out of 18 cases with MLD, one patient was found homozygous for the Pd allele and the other patient was found heterozygous.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

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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Bu Makaleye Atıf Yap

EMRE, S., RENDA, Y., TOPÇU, M., TERZİOĞLU, M. (2022). Arylsulfatase a pseudodeficiency incidence in Turkey. Turkish Journal of Pediatrics, Cilt: 42 - Sayı: 2, 115–117. https://ajindex.com/articles/613342

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