Literature DB >> 30890857

Association of eNOS 27-bp VNTR, 894G>T and 786T>C polymorphisms with susceptibility to Legg-Calve-Perthes Disease in Iranian children.

Mohammad Reza Azarpira1, Mohammad Mahdi Ghilian1, Mohammad Reza Sobhan2, Masoud Mahdinezhad-Yazdi2, Kazem Aghili3, Hossein Ahrar3, Hossein Neamatzadeh4,5.   

Abstract

BACKGROUND: The aim of this study was to analyze the association of eNOS polymorphisms with risk of Legg-Calve-Perthes Disease (LCPD).
METHODS: The study comprised of 45 LCPD patients and 55 controls. The eNOS polymorphisms were genotyped with PCR and by PCR-RFLP.
RESULTS: The eNOS 894G > T and -786T > C polymorphisms were significantly associated with an increased risk of LCPD. However, there was no significant association between eNOS 27-bp VNTR polymorphism and LCPD risk.
CONCLUSION: Our results suggest that the eNOS 894G > T and -786T > C polymorphisms may be a risk factor for LCPD in Iranian children, but not 27-bp VNTR polymorphism.

Entities:  

Keywords:  Legg-Calve-Perthes disease; Nitric oxide synthase; Polymorphism

Year:  2019        PMID: 30890857      PMCID: PMC6403418          DOI: 10.1016/j.jor.2019.02.024

Source DB:  PubMed          Journal:  J Orthop        ISSN: 0972-978X


  26 in total

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Journal:  Orphanet J Rare Dis       Date:  2022-03-09       Impact factor: 4.123

Review 2.  Legg-Calvé-Perthes disease overview.

Authors:  Armando O Rodríguez-Olivas; Edgar Hernández-Zamora; Elba Reyes-Maldonado
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3.  Investigation of eNOS G894T Gene Polymorphism in Patients with Pseudoexfoliation Syndrome: A Preliminary Study.

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