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  | ARTICLES | Am. J. innov. res. appl. sci. Volume 10,  Issue 4, Pages 139-147 (April 2020)
Revew Article 2
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American Journal of innovative
Research & Applied Sciences 
ISSN  2429-5396 (Online)
OCLC Number: 920041286
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| IMPACT FACTOR AND INDEXING | | PUBLICATION FEE |
| APRIL | VOLUME 10 | N° 4 | 2020 |
| Info-AJIRAS-® Journal ISSN 2429-5396 (Online) / Reference  CIF/15/0289M |
  American Journal of Innovative Research & Applied Sciences
*Corresponding author Author & Copyright Author © 2020: | Fadoua Bouzid  |. All Rights Reserved. All articles published in American Journal of Innovative Research and Applied Sciences are the property of Atlantic Center
Research Sciences, and is protected by copyright laws CC-BY. See: http://creativecommons.org/licenses/by-nc/4.0/
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*Correspondant author and authors Copyright © 2020:

|  Fadoua Bouzid 1* | Ilham Benyamna 1 | Abdelhamid Elmousadik 1 | Abdellah Moustaine | and | Najat Alif  1 |.

Affiliation.

1Laboratory of Biotechnologies and Valorization of Natural Resources | School of Sciences | IBN Zohr University | Agadir | Morocco |
2. Pediatric practice | Agadir | Morocco |


This article is made freely available as part of this journal's Open Access: ID | Fadoua-Ref.7-ajira190320 |
Abstract

Bachground: Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease caused by the deficiency of the α-L-iduronidase (IDUA) enzyme. This deficiency leads to the accumulation of dermatan sulfate and heparan sulfate. Objective: The aim of this study is to detect IDUA mutational spectrum in 14 Moroccan patients with MPS I. Methods: Diagnosis of MPS I was confirmed by a biochemical study. The molecular analysis was performed by direct sequencing of IDUA gene from DNA patients’ sample, their parents and control subjects. Result: In this series, we have detected the previously reported mutation p.P533R at homozygous state in 92.85% of studied patients and an unreported deletion mutation p.P515fs (c.1545delC) at heterozygous state in one patient, showing the Hurler phenotype. In addition, five polymorphisms in the homozygous or heterozygous states including two new variants were detected of studied patients. These non-pathogenic variants indicate a high degree of allelic heterogeneity explaining different observed phenotypes.
Keywords:
Mucopolysaccharidosis type I; IDUA gene; p.R533P; p.P515fs; polymorphisms
MOLECULAR ANALYSIS OF MUCOPOLYSACCHARIDOSIS TYPES I IN MOROCCO: IDENTIFICATION OF NOVEL MUTATION AND FIVE POLYMORPHISMS

|  Fadoua Bouzid 1* | Ilham Benyamna 1 | Abdelhamid Elmousadik 1 | Abdellah Moustaine | and | Najat Alif  1 |.  Am. J. innov. res. appl. sci. 2020; 10(4):139-147.

    | PDF FULL TEXT |  | XML FILE  |  | Received | March 9, 2020 | | Accepted | March 19, 2020 |  | Published | April 1, 2020 |