Molecular Genetic Testing in Pediatric and Adult Neurology in Iraq: New Experience and Challenges from a Developing Country

Author:

Saadi Nebal Waill1ORCID,Yassin Batool Ali Ghalib2,Makhseed Nawal3,Hadi Ameer Shaker4

Affiliation:

1. Department of Pediatric Neurology, Children Welfare Teaching Hospital, College of Medicine, University of Baghdad, Baghdad, Iraq

2. Department of Community Medicine, College of Medicine, University of Baghdad, Baghdad, Iraq

3. Department of Paediatric, Al Jahra Hospital, Al Jahra, Kuwait

4. Department of Neurology, Baghdad Teaching Hospital, Baghdad, Iraq

Abstract

AbstractInherited neurological disorders are reasonably common in pediatric and adult neurology practices. Genetic testing for such disorders does carry promise, but is fraught with challenges and difficulties. This study was conducted to assess the utility of genetic testing in a cohort of 200 patients who had neurological disorders, suspected to be of inherited origin, and for whom molecular genetic testing was requested during the period 2014 to 2019. Two hundred and eight tests were ordered. The characteristics of that practice were reviewed. Further, we summarized the challenges and highlighted the concerns that were raised. The medical records of 200 patients were retrieved and reviewed to assess the demographic characteristics of the cohort, their clinical presentation, genetic test requested for each, and the interpretation of the test results.

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Reference23 articles.

1. Genetics of hereditary neurological disorders in children;Y Huang;Transl Pediatr,2014

2. Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report;H Hamamy;Genet Med,2011

3. Molecular characterization of dystrophin gene in Iraqi patients with muscular dystrophy;A TR Al-Hadithi;J Fac Med Baghdad,2014

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