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Iman S. Abumansour MBBS

Consultant, Medical Genetics & Metabolic
Children's Health Center

Years of Experience: 12

x SURGEON
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En Ar

Education

Medical School

2008

Bachelor’s Degree in Medicine and Surgery

Umm Al-Qura University, Makkah, Saudi Arabia

Residency

2016

Resident, Medical Genetics

University of Manitoba, Medical Genetics Department Health Sciences Centers, Canada

Membership

  • The Royal College of Physicians and Surgeons of Canada

License

  • Saudi Commission for Health Specialties

Work Experience

2021 – Present

Consultant, Medical Genetics & Metabolic

International Medical Centre in Jeddah, Saudi Arabia

2019 – Present

Consultant, Medical Genetics

King Faisal Specialist Hospital & Research Center in Jeddah, Saudi Arabia

2017 – Present

Assistant Professor in Medical Genetics Department

Umm Al-Qura University, Makkah, Saudi Arabia

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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