Medical Genetics
First appointment
For referrals, please see details below.
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Medical Genetics
Medical Genetics services are provided by a multidisciplinary team of geneticists, genetic counsellors, pediatricians, dieticians, nurses, molecular geneticists and cytogeneticists. The goal is to diagnose, treat and prevent congenital and hereditary disorders. We provide specialized services in general genetics, cancer genetics, biochemical genetics and prenatal diagnosis, and offer community screening for common Ashkenazi Jewish disorders. We are a referral centre for hereditary metabolic conditions. We provide preconception, prenatal and postnatal evaluation, as well as risk assessment and counselling.
Services
General Genetics
The General Genetics team consists of geneticists and genetic counselors who evaluate adults and children who are at risk for, or suspected to have, a genetic syndrome or a disorder with a genetic component. Patients receive genetic evaluations and genetic counselling that includes the discussion, organization and interpretation of genetic tests for inherited conditions. We work closely with other specialties in the hospital as well as other healthcare providers in the community to ensure that the child’s needs are addressed. For more information, visit this page.
Biochemical Genetics
The metabolic program at the MUHC provides a comprehensive program for the diagnosis and biochemical management of patients with inborn errors of metabolism (IEM). We see a broad range of patients covering all ages from birth to adulthood and all aspects of metabolic disease.
Prenatal diagnosis
Our genetic counsellors and medical geneticists see patients for genetic counselling and consultation for a variety of indications in pregnancy, including a fetal malformation or soft marker identified on ultrasound, a fetal chromosome abnormality, a positive prenatal screening result, a teratogen exposure or a family history of a genetic condition. Most referrals to our service are considered urgent since there is an ongoing pregnancy. Please visit this page for more information.
Cancer Genetics
The cancer genetics service works in close partnership with its sister service at the Jewish General Hospital to provide genetic counselling services for individuals and families at increased risk of hereditary cancers, both in pediatric and adult patients.
Ashkenazi Jewish genetic screening services
The Ashkenazi Jewish genetic screening services provide genetic counselling and screening for all individuals and couples who are of Ashkenazi Jewish descent.
Huntington’s Disease Clinic
Our clinic provides education and support to individuals and families touched by Huntington’s Disease, from genetic consultation to predictive testing.
Referrals
Referring physicians can fax their consultation request to 514-412-4296 or send it to [email protected].
Patients do not need a physician’s referral to be seen in our service. To schedule an appointment, please fax or email us the following information about the patient:
- Reason for referral
- First name, last name
- Date of birth
- Medicare number and expiration date
- Address
- Phone number
Your first appointment
You have been asked to be seen by Genetics because you or a family member has a health condition that has required medical attention that could have an impact on other family members. Our doctors and genetic counsellors will try to find the reason for these problems.
Laboratory and service affiliates
Our laboratories perform various specialized diagnostic tests:
- Molecular genetics laboratory
- Biochemical genetics laboratory (BCG)
- Cytogenetics laboratory (affiliate)
Team
Physicians
Nancy Braverman,
MD, MS, FACMG
Daniela Buhas,
MD, FRCPC, FCCMG
Isabelle De Bie,
MD, PhD, FRCPC, FCCMG
June Ortenberg,
MD
David Rosenblatt,
MD
Laura Russell,
MD, FACMG
Geneviève Bernard,
MD, MSc, FRCPC
Maria Daniela D’Agostino
MD, MSc, FRCPC
Yannis Trakadis,
MD, MSc, FRCPC, FCCMG
Genetic Counsellors
Stella Drury
MSc, CCGC, CGC
Stephanie Fox
MSc, CCGC, CGC
Lidia Kasprzak
MSc, CGC
Laura Palma
MSc, CCGC, CGC
Guillaume Sillon
MSc, CGAC
Laura Whelton
MSc, CCGC, CGC
Marilyn Richard
MSc, CGC, CCGC
Nancy Anoja
MSc, CCGC
Karen Canales
CCGC
Laurence Baret
CCGC
Nutritionist
Marie Lefrançois
Dt.P./ R.D.
Metabolic Nutritionist Nurse
Lina Moisan,
BscN
Clinical Manager, Medical Genetics
Mélanie Langelier
RN, MSN
Resources
Referral forms and questionnaires
- Medical genetic referral form
- Connective tissue disorder referral form
- Medical genetics pediatric questionnaire
- Cancer screening medical genetics questionnaire
General information
- About Kids Health, Genetics – SickKids
Support Groups
- Regroupement québécois des maladies orphelines
- Orphanet, the portal for rare diseases and orphan drugs
- Regroupement pour la trisomie 21
- Association de la Neurofibromatose du Québec (English site)
- Société Huntington du Québec
Book
- Vivre avec une maladie génétique, by Marcela Gargiulo, in collaboration with Martine Salvador