Vickie Zurcher, MD
Cleveland Clinic Main Campus
Treatment & Services
- Genetic Counseling
- Genetic Evaluation
- Genomic Medicine
- Reproductive Risk Assessment & Counseling
Specialty in Diseases & Conditions
- Adolescents with Developmental Disabilities
- Angelman Syndrome
- Beckwith-Wiedemann Syndrome (BWS)
- Birth Defects
- Chromosome Abnormalities
- Cleft Lip
- Cleft Palate
- Congenital Anomalies
- Congenital Hand Differences
- Congenital Head and Neck Disease
- Congenital Head And Neck Masses
- Congenital Malformations
- Congenital Renal Malformations
- Congenital Vascular Lesions
- Down Syndrome
- Dysplastic Kidney
- Epidermal Nevus Syndrome
- Family History of Genetic Disorders
- Genetic Abnormalities
- Genetic Skin Diseases
- Hamartoma Conditions
- Incontinentia Pigmenti
- Intersex Conditions
- Joubert Syndrome
- Kidney & Bladder Birth Defects
- Klinefelter Syndrome
- Klippel-Trenaunay Syndrome (KTS)
- Malformations Of Cortical Development
- McCune-Albright Syndrome
- Noonan Syndrome
- Pediatric Birthmark
- Pediatric Craniofacial Disorders
- Pigment Abnormalities
- Rett Syndrome
- Septo-optic Dysplasia (SOD)
- Skin Conditions
- Skin Lesions
- Skin Problems in Children
- Speech/language Delay
- Spina Bifida
- Tuberous Sclerosis Complex
- Turner Syndrome
- Vascular Anomalies
- Vascular Malformations
- Vestibular Schwannomas
- Williams Syndrome
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About Vickie Zurcher, MD
Vickie Lee Zurcher, MD, is a Clinical Geneticist with the Cleveland Clinic's Genomic Medicine Institute.
Dr. Zurcher is board certified in pediatrics and clinical genetics. She completed her undergraduate degree at The College of Wooster in Wooster, Ohio, and she earned her medical degree from The University of Cincinnati College of Medicine in Cincinnati, Ohio. Her post-graduate training includes a pediatric internship and residency at The Children’s Memorial Hospital (now Lurie Children's Hospital) in Chicago, Illinois and a clinical genetics fellowship at Case Western Reserve University in Cleveland, Ohio.
Dr. Zurcher is a Founding Fellow of the American College of Medical Genetics, a Fellow of the American Academy of Pediatrics, and a member of the American Society of Human Genetics.
Dr. Zurcher has been an author on a number of articles in peer-reviewed journals and has co-authored abstracts and presentations at professional association meetings.
Her specialty interests include neurofibromatosis and other neurocutaneous disorders, dysmorphic syndromes, congenital malformations, chromosomal abnormalities, and genetic skin diseases.
Education & Professional Highlights
Education & Fellowships
Fellowship - University Hospitals/Case Western Reserve University - Center for Human Genetic
Cleveland, OH USA
Residency - Children's Memorial Hospital - demolished. Replaced by Lurie Children's Hospita
Chicago, IL USA
Internship - Children's Memorial Hospital
Chicago, IL USA
Medical Education - University of Cincinnati College of Medicine
Cincinnati, OH USA
Undergraduate - College of Wooster
Major biology. Minor chemistry.
Wooster, OH USA
- Medical Genetics and Genomics - Clinical Genetics
Congenital malformations Dysmorphic syndromes Chromosomal abnormalities Neurofibromatosis and other neurocutaneous syndromes Genetic skin disorders Reproductive risk assessment and counseling
Awards & Honors
Innovations & Patents
- American College of Medical Genetics and Genomics
- American Academy of Pediatrics
- American Society of Human Genetics
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As of 6/6/2022, Dr. Zurcher has reported no financial relationship with industry that is applicable to this listing. In general, patients should feel free to contact their doctor about any of the relationships and how the relationships are overseen by Cleveland Clinic. To learn more about Cleveland Clinic's policies on collaborations with industry and innovation management, go to our Integrity in Innovation page.
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