Ian MacDonald, MD, CM, FCCMG, FRCSC - Ophthalmology

Dr. MacDonald is a professor and chair of the Department of Ophthalmology at the University of Alberta, in Edmonton, Alberta. His current research focus is translational research in eye genetics.

Board Certifications

Canadian College of Family Physicians—1981
Fellow, Canadian College of Medical Genetics—1986
Fellow in Ophthalmology, Royal College of Physicians and Surgeons of Canada—1989

Healthwise Knowledgebase Topics Reviewed

Glaucoma
Pink Eye
Colour Blindness
Styes and Chalazia
Age-Related Macular Degeneration
Blocked Tear Ducts
Cataracts

Education

MDCM: McGill University, Montreal, QC, 1979
Residency: Family Medicine, Queen Elizabeth Hospital, Montreal, QC, 1979–1981
Fellowship: Clinical Genetics and Cytogenetics, Children's Hospital of Eastern Ontario; Biochemical Genetics, Hospital for Sick Children; Molecular Genetics, Queen's University, Kingston, Ottawa and Toronto, ON, 1983–1984
Research Fellowship: Clinical Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, 1984–1985
Fellowship: Medical Research Council of Canada, University of Ottawa, Ottawa, ON, 1985–1986
Residency: Ophthalmology, Ottawa Civic Hospital, Ottawa General Hospital, and Children's Hospital of Eastern Ontario (Chief Resident, 1988–1989), Ottawa, ON, 1986–1989

Academic Appointments

Clinical Professor, Department of Medical Genetics, University of Calgary, Calgary, AB, 1998–present
Associate Professor, Department of Medical Genetics, University of Alberta, Edmonton, AB, 1996–present
Professor and Chair, Department of Ophthalmology, University of Alberta, Edmonton, AB, 1992–present

Hospital Affiliations

Royal Alexandra Hospital, Edmonton, AB

Professional Affiliations

Canadian Ophthalmological Society
American Academy of Ophthalmology
American Society of Human Genetics
Canadian Association of Pediatric Ophthalmologists
International Society for Clinical Electrophysiology of Vision
International Society for Genetic Eye Diseases
Ophthalmological Society of Alberta

Selected Publications

  1. Tran M, Bhargava R, MacDonald IM (2001). Leber hereditary optic neuropathy, progressive visual loss, and multiple sclerosis-like symptoms. American Journal of Ophthalmology, 132(4): 591–593.
  2. MacDonald IM, Mah DY (2000). Summary of heritable ocular disorders and selected systemic conditions with eye findings. Ophthalmic Genetics, 21(1): 29–49.
  3. Mah DY, Wong PW, Edwards A, MacDonald IM (1998). Recent advances in the genetics of macular dystrophies. Canadian Journal of Ophthalmology, 33: 135–143.
  4. MacDonald IM (1994). Recent advances in the molecular genetics of inherited eye disorders. Canadian Journal of Ophthalmology, 29: 256–262.

Financial Disclosure

This reviewer reported no financial conflicts.




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