Overview
Sylvie Langlois practices in Vancouver, Canada. Ms. Langlois is rated as an Advanced expert by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Trisomy 18, Trisomy 13, Chromosome 13q Duplication, and Down Syndrome.
Her clinical research consists of co-authoring 85 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 4 articles in the study of Chromosome 13q Duplication.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
1 Clinical Trials
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Chromosome 13q DuplicationMs. Langlois isAdvanced. Learn about Chromosome 13q Duplication.
- Down SyndromeMs. Langlois isAdvanced. Learn about Down Syndrome.
- Trisomy 13Ms. Langlois isAdvanced. Learn about Trisomy 13.
- Trisomy 18Ms. Langlois isAdvanced. Learn about Trisomy 18.
- Experienced
- Acute Lymphoblastic Leukemia (ALL)Ms. Langlois isExperienced. Learn about Acute Lymphoblastic Leukemia (ALL).
- Adult T-Cell LeukemiaMs. Langlois isExperienced. Learn about Adult T-Cell Leukemia.
- AnencephalyMs. Langlois isExperienced. Learn about Anencephaly.
- AniridiaMs. Langlois isExperienced. Learn about Aniridia.
- Brachydactyly Mononen TypeMs. Langlois isExperienced. Learn about Brachydactyly Mononen Type.
- Caffey DiseaseMs. Langlois isExperienced. Learn about Caffey Disease.