Literature DB >> 29333903

The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System.

Mahmoud Reza Ashrafi1, Zahra Rezaei1, Morteza Heidari2, Sedigheh Nikbakht1, Reza Azizi Malamiri3, Mahmoud Mohammadi1, Gholam Reza Zamani1, Reza Shervin Badv1, Parastoo Rostami4, Mojtaba Movahedinia1, Mostafa Qorbani5, Man Amanat1, Ali Reza Tavasoli1.   

Abstract

Childhood leukodystrophies are a fast-growing field of pediatric neurology practice. Epidemiologic studies on the incidence of these disorders in children show different results. This is the first report of childhood leukodystrophies incidence from Iran. The enrolled patients were recruited from the neurometabolic bioregistry system that was organized in 2010 in the Children's Medical Center, Tehran, Iran. Herein is reported the incidence rate of leukodystrophies in those patients who were residents of 2 big popular provinces near Iran's capital city Tehran, with an average child population of 2 988 800 children. Ninety cases of leukodystrophies from Tehran and Alborz provinces who were registered between 2010 and 2016 in the bioregistry system were enrolled in this study. The annual incidence of inherited white matter disorders was 3.01/100 000, the highest number compared with those found in other studies using similar methods throughout the world. One of the main cause of this higher incidence could be the higher number of consanguineous marriages in Iran.

Entities:  

Keywords:  children; genetics; inborn error of metabolism; leukodystrophy; magnetic resonance imaging (MRI)

Mesh:

Year:  2018        PMID: 29333903     DOI: 10.1177/0883073817751804

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  4 in total

1.  Novel and known morbidities of leukodystrophies identified using a phenome-wide association study.

Authors:  Joshua L Bonkowsky; Jacob Wilkes; Jian Ying; Wei-Qi Wei
Journal:  Neurol Clin Pract       Date:  2020-10

Review 2.  Probable Vanishing White Matter Disease: A Case Report and Literature Review.

Authors:  Endayen Deginet; Robel Tilahun; Solomon Bishaw; Konjit Eshetu; Ayalew Moges
Journal:  Ethiop J Health Sci       Date:  2021-11

3.  Association of Diagnosis of Leukodystrophy With Race and Ethnicity Among Pediatric and Adolescent Patients.

Authors:  Joshua L Bonkowsky; Jacob Wilkes; Tyler Bardsley; Veronica M Urbik; Greg Stoddard
Journal:  JAMA Netw Open       Date:  2018-11-02

4.  ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants.

Authors:  Ali Zare Dehnavi; Erfan Heidari; Maryam Rasulinezhad; Morteza Heidari; Mahmoud Reza Ashrafi; Mohammad Mahdi Hosseini; Fatemeh Sadeghzadeh; Mohammad-Sadegh Fallah; Noushin Rostampour; Amir Bahraini; Masoud Garshasbi; Ali Reza Tavasoli
Journal:  Hum Genomics       Date:  2021-07-19       Impact factor: 4.639

  4 in total

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