donate icon DONATE
Dinesh Choudhry

Philippe Campeau, MD, FRCP(C), FAAP

Specialties
  • Medical Genetics
Areas of Care:
Location(s):
Languages Spoken:
  • English
  • French

Philippe Campeau, M.D., FRCP(c), FCCMG, specialized in medical genetics to better understand how diseases occur at a basic level, and to eventually develop more targeted therapies to help affected children. His focus on skeletal dysplasias developed as he trained under Brendan H. Lee at the Baylor College of Medicine in Houston Texas, before returning to Montreal in 2013.

Pediatric Care

Specialties

CTA Icon Request an Appointment
star icon Refer a Patient
Appointments with specific providers are based on availability and scheduling.

WHERE I PROVIDE CARE

Pediatric specialty care for children throughout Montreal and beyond
More About This Location
Canada hospital exterior

More About Me

Board Certifications
  • The Royal College of Physicians and Surgeons of Canada, Medical Genetics, Medical Genetics - General
Education and Training

Medical Education
Université Laval
Québec, QC
Canada
6/30/2003

Residency
McGill University
Montréal, QC
Canada
6/30/2008

Fellowship
Baylor College of Medicine
Houston, TX
United States of America
3/1/2013

Academic Positions and Locations

Université de Montréal
Associate Clinical Professor

Leadership and Memberships
  • 2019-Present: Deputy Head, Musculoskeletal Diseases and Rehabilitation Research Axis, CHU Sainte-Justine Research Center
  • 2018-Present: Co-PI, Rare Diseases Models and Mechanisms Network
  • 2014-Present: Local PI: A Multicenter, Multinational, Observational Morquio A Registry Study (MARS). (ClinicalTrials.gov/show/NCT02294877)
  • 2019-Present: Local PI: A Multi-center, Longitudinal, Observational Study of Children with Achondroplasia. (ClinicalTrials.gov/show/NCT03875534)
Editorial Positions
  • 2021-Present: European Journal of Human Genetics
Awards and Honors
  • 2014, CIHR Maud Menten New Investigator Award
  • 2018, CIHR Clinician Scientist Award (Phase 2 Renewal)
  • 2018, FRSQ Clinical Research Scholar Award (Junior 2 Level)
Scholarly Activities
Academic Works and Presentations
  • Presentation: ASHG Annual Meeting - Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1 (2019)

Next Steps

Request an Appointment

Families and caregivers seeking treatment should start by contacting us for an appointment.
Get Started

Log in to the Patient Portal

Parents and guardians of existing patients can email, request records, schedule appointments and more.
Log in Now

Refer a Patient

Physicians and healthcare providers can request appointments, start transfers or contact us with questions.
Send Referral