(Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children)
Mucopolysaccharidosis (MPS) is a rare heterogenous progressive genetic disorder, which is a subset of lysosomal storage diseases with a consequence of glycosaminoglycans building-up inside the lysosomes which attributed to enzymes absence or deficiency. This study was aimed to identify mutations t...
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| Format: | Article |
| Language: | English |
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College of Pharmacy University of Baghdad
2024-12-01
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| Series: | Iraqi Journal of Pharmaceutical Sciences |
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| Online Access: | https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/2845 |
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| author | Furqan Abdulelah Mohammed M. Mohammed Rabab Hassan Baaker |
| author_facet | Furqan Abdulelah Mohammed M. Mohammed Rabab Hassan Baaker |
| author_sort | Furqan Abdulelah |
| collection | DOAJ |
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Mucopolysaccharidosis (MPS) is a rare heterogenous progressive genetic disorder, which is a subset of lysosomal storage diseases with a consequence of glycosaminoglycans building-up inside the lysosomes which attributed to enzymes absence or deficiency. This study was aimed to identify mutations that associated with mucopolysaccharidosis of Iraqi children in different Iraqi metabolic centers. While in concerning to the genetic study, the eligible patients who had no genetic analysis and who are not received hematopoietic stem cells transportation were enrolled in this study for molecular confirmation of mucopolysaccharidosis disorders and reporting the existence of any new variants among Iraqi patients. Consequently, the study reports various SNPs are responsible for different MPS types, for instance, there are seven SNPs within IDAU gene of MPS I Iraqi patients, the most frequent one was rs794726877 which accounts for missense c.152G>A. Finally, the study recommends establishment of awareness programs for affected families regarding the genetic conditions, inheritance pattern and potential availability of reproductive options such as In Vitro Fertilization (IVF), educate the population at risk about the risk of genetic disease transmission as a result of inbreed marriage and necessity of availability of prenatal screening and pregnancy termination option in Iraq.
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| format | Article |
| id | doaj-art-209354d84e954af28c72d632e4a0ca5c |
| institution | OA Journals |
| issn | 1683-3597 2521-3512 |
| language | English |
| publishDate | 2024-12-01 |
| publisher | College of Pharmacy University of Baghdad |
| record_format | Article |
| series | Iraqi Journal of Pharmaceutical Sciences |
| spelling | doaj-art-209354d84e954af28c72d632e4a0ca5c2025-08-20T01:58:44ZengCollege of Pharmacy University of BaghdadIraqi Journal of Pharmaceutical Sciences1683-35972521-35122024-12-0133410.31351/vol33iss4pp102-114(Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children)Furqan Abdulelah0Mohammed M. Mohammed 1Rabab Hassan Baaker2College of Dentistry, Al-Bayan University, Baghdad, IraqCollege of Pharmacy, Mustansiriyah University, Baghdad, IraqCollege of Medicine, Mustansiriyah University, Baghdad, Iraq Mucopolysaccharidosis (MPS) is a rare heterogenous progressive genetic disorder, which is a subset of lysosomal storage diseases with a consequence of glycosaminoglycans building-up inside the lysosomes which attributed to enzymes absence or deficiency. This study was aimed to identify mutations that associated with mucopolysaccharidosis of Iraqi children in different Iraqi metabolic centers. While in concerning to the genetic study, the eligible patients who had no genetic analysis and who are not received hematopoietic stem cells transportation were enrolled in this study for molecular confirmation of mucopolysaccharidosis disorders and reporting the existence of any new variants among Iraqi patients. Consequently, the study reports various SNPs are responsible for different MPS types, for instance, there are seven SNPs within IDAU gene of MPS I Iraqi patients, the most frequent one was rs794726877 which accounts for missense c.152G>A. Finally, the study recommends establishment of awareness programs for affected families regarding the genetic conditions, inheritance pattern and potential availability of reproductive options such as In Vitro Fertilization (IVF), educate the population at risk about the risk of genetic disease transmission as a result of inbreed marriage and necessity of availability of prenatal screening and pregnancy termination option in Iraq. https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/2845genetic variants, Iraqi children, mucopolysaccharidosis, single nucleotide polymorphism. |
| spellingShingle | Furqan Abdulelah Mohammed M. Mohammed Rabab Hassan Baaker (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) Iraqi Journal of Pharmaceutical Sciences genetic variants, Iraqi children, mucopolysaccharidosis, single nucleotide polymorphism. |
| title | (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) |
| title_full | (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) |
| title_fullStr | (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) |
| title_full_unstemmed | (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) |
| title_short | (Genetic Study of Mucopolysaccharidosis in A Sample of Iraqi Children) |
| title_sort | genetic study of mucopolysaccharidosis in a sample of iraqi children |
| topic | genetic variants, Iraqi children, mucopolysaccharidosis, single nucleotide polymorphism. |
| url | https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/2845 |
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