Alberta – Dr. Aneal Khan, Assistant Professor of Medical Genetics and Pediatrics
Alberta Children’s Hospital, University of Calgary

Dr. Khan is a specialist in inborn errors of metabolism, a medical geneticist and pediatrician. He works out of the Alberta Children’s Hospital in Calgary, Alberta and his practice is 80% clinical and 20% research. Dr. Khan’s research is focused on interventions in patients with rare diseases. Past work includes patients on enzyme replacement therapy trials. He has a special interest in interventional therapies, mitochondrial diseases, lysosomal storage diseases, bone disease and cardiomyopathies.

Dr. Aneal Khan

Alberta Children’s Hospital, University of Calgary
3rd Floor Metabolic Clinic
2888 Shaganappi Trail NW
Calgary, Alberta, Canada, T3B 6A8
Tel: (403)-955-5030 Fax: (403)-955-3091

Manitoba – Dr. Cheryl Rockman-Greenberg and Dr. Aziz Mhanni Genetics and Metabolism, HSC Winnipeg

Both Dr. Greenberg, and Dr. Mhanni are trained in clinical genetics, and provide ongoing diagnostic and support care to Manitoba families dealing with Mitochondrial Diseases.

Dr. Cheryl Rockman-Greenberg
Pediatrics and Child Health
Children’s Hospital
CE208 – 840 Sherbrook St.
Winnipeg, MB R3A 1S1
Phone: (204) 787-2441
Admin Assistant: (204) 787-1970

A. Mhanni, Ph.D. (Manitoba) MD, FRCPC, FCCMG, FACMG
Assistant Professor, Pediatrics & Child Health; Biochemistry & Medical Genetics
Clinical Genetics and Inborn Errors of Metabolism. Research focus is in epigenetics and how it relates to human disorders and DNA methylation role in early developmental processes and its relationship to specific birth defects such as conotruncal anomalies of the heart.
Member of the Medical Genetics Research Group
Tel: (204) 787-2958; Pager: (204) 932-0788

Ontario – Dr. Annette Feigenbaum: Hospital for Sick Children, Clinical and Metabolic Genetics Clinic

THe Clinical and Metabolic Genetics Clinic specializes in pediatric patients with metabolic and genetic disorders, including Mitochondrial Disease.

Hospital for Sick Children, Clinical and Metabolic Genetics Clinic
Dr. Annette Feigenbaum

The Hospital for Sick Children, Division of Clinical and Metabolic Genetics, 555 University Avenue, Toronto, Ontario, M5G 1X8, Tel: 416.813.6390, Fax: 416.813.5345

Ontario – Dr. Mark Tarnopolsky: McMaster Children’s Hospital / Hamilton Health Sciences, Chair in Neuromuscular Disorders

Clinic: Neuromuscular and Neurometabolic Clinic

Dr. Tarnopolsky is an exceptional clinician and researcher with a passion for both helping patients with mitochondrial disease, and doing research to find better treatments and a cure. Dr. Tarnopolsky treats both pediatric and adult patients.
The Neuromuscular and Neurometabolic Centre at McMaster the first clinic in Canada that diagnoses, treats and cares for people with Mitochondrial disease throughout their life span.
His clinic at McMaster Children’s Hospital in Hamilton, Ontario, is the Neuromuscular and Neurometabolic Clinic, Contact and referral information is provided on the clinic’s McMaster Children’s Hospital web page:

Neuromuscular and Neurometabolic Clinic, McMaster Children’s Hospital
Dr. Tarnopolsky Chair in Neuromuscular Disorders

Hamilton Health Sciences, 1200 Main Street West, Hamilton, ON L8S 4J9
Phone: 905-521-7933

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