Bachelor’s Degree in Medicine and Surgery
Umm Al-Qura University, Makkah, Saudi Arabia
Back Doctor Details
Iman S. Abumansour MBBS
Consultant, Medical Genetics & Metabolic
Children's Health Center
Years of Experience: 12
SURGEON
Languages
Languages:
- English
- Arabic
Education
2008
Medical School
2008
2016
Residency
2016
Resident, Medical Genetics
University of Manitoba, Medical Genetics Department Health Sciences Centers, Canada
Work Experience
2021
2021 - Present
Consultant, Medical Genetics & Metabolic
International Medical Centre in Jeddah, Saudi Arabia
2019
2019 - Present
Consultant, Medical Genetics
King Faisal Specialist Hospital & Research Center in Jeddah, Saudi Arabia
2017
2017 - Present
Assistant Professor in Medical Genetics Department
Umm Al-Qura University, Makkah, Saudi Arabia
Membership
- The Royal College of Physicians and Surgeons of Canada
Publications
- Sep 2019- TOTAL ANOMALOUS PULMONARY VENOUS DRAINAGE IN ASSOCIATION WITH KAUFMAN SYNDROME (Published, Co-Author)
- Jun 2019- MORQUIO BDISEASE:CLINICAL AND GENETIC CHARACTERSITICS OF A DISTINCT GLB1-RELATED DYSOSTOSIS MULTIPLEX (Published, First Author)
- Jan 2016-IDENTIFICATION OF A RECURRENT FRAMESHIFT MUTATION AT THE LDLREXON 14(C.2027DELG,P.(G676AFS*33) CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SAUDI ARAB HOMOZYGOUS CHILDREN (Published, Co- authorn Genomics 2016)
- Aug 2015- ARL6IP6. A SUSCEPTIBILITY LOCUS FOR ISCHEMIC STROKE,IS MUTATED IN A PATIENT WITH SYNDROMIC CUTIS MARMORATA TELANGIECTATICA CONGENITA (Published, First author Human Genetics 2015)
- June 2015- CLINICAL UTILITY OF THE MENDELIOME ACROSS DISCIPLINES OF MEDICINE. (Published, Co-author
Genome Biology 2015) - Oct 2015- PRENATAL DIAGNOSIS OF WALKER WARBURG SYNDROME USING SNP ARRAY: AC LINICAL EXPERIENCE FROM THREE RELATED PALESTINIAN FAMILIES WITH CONGENITAL HYDROCEPHALUS (Published, First Author - American Journal of Perinatology 2015)
- Nov 2014-IDENTIFICATION OF A NOVEL NONSENSE VARIANT C.1332DUP,P.(D445*)IN THE LDLRGENE THAT CAUSES
FAMILIAL HYPERCHOLESTEROLEMIA. (Published, Co-author - Human Genome Variation 2014) - March 2013-LISSENCEPHALY WITH BRAINSTEM AND CEREBELLAR HYPOPLASIA AND CONGENITAL CATARACTS (Published, 1st Author - Journal of Child Neurology 2014)
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