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Office
10104 Frederick Ave
Kensington, MD 20895Phone+1 301-962-6441
Summary
- Dr. Donna Krasnewich, MD is a board certified medical geneticist in Kensington, Maryland. She is currently licensed to practice medicine in Maryland, District of Columbia, and Virginia.
Education & Training
National Capital ConsortiumResidency, Pediatrics, 1989 - 1991
Children's National HospitalResidency, Pediatrics, 1987 - 1989
University of MinnesotaInternship, Transitional Year, 1986 - 1987
Wayne State University School of MedicineClass of 1986
Certifications & Licensure
DC State Medical License 1989 - 2018
MD State Medical License 1996 - 2018
VA State Medical License 1900 - 1900- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Pediatrics Pediatrics
Publications & Presentations
PubMed
- Neurodevelopmental profiles of 14 individuals with phosphomannomutase deficiency (PMM2-CDG).Tara Weixel, Dee Adedipe, Glennis Muldoon, Christina Lam, Donna Krasnewich
Journal of Inherited Metabolic Disease. 2024-08-06 - 4 citationsA Participatory Framework for Plain Language Clinical Management Guideline Development.Rita Francisco, Susana Alves, Catarina Gomes, Pedro Granjo, Carlota Pascoal
International Journal of Environmental Research and Public Health. 2022-10-19 - 7 citationsOne is the loneliest number: genotypic matchmaking using the electronic health record.Elly Brokamp, Mary Koziura, John A. Phillips, Leigh Anne Tang, Joy D. Cogan
Genetics in Medicine. 2021-07-06
Grant Support
- Clinical Heterogenity In Patients With Congenital DisordNational Human Genome Research Institute2002–2006
- Characterization Of A Familial Presenile Dementia With NNational Human Genome Research Institute2002–2005
- Clinical Heterogenity:Congenital Glycosylation DisordersNational Human Genome Research Institute2004
- Heterogenity In Patients With Congenital GlycosylatioinNational Human Genome Research Institute2003
- Familial Presenile Dementia W/ Neuronal Inclusion BodiesNational Human Genome Research Institute2003
- Heterogenity In Congenital Disorders Of GlycosylationNational Human Genome Research Institute2001
- Familial Presenile Dementia With Neuronal Inclusion BodyNational Human Genome Research Institute2001
- Clinical Heterogenity In Patients With Congenital Disorders Of GlycosylationNational Human Genome Research Institute2000
- Characterization Of A Familial Presenile DementiaNational Human Genome Research Institute2000
- Clinical Heterogenity In Patients With Carbohydrate Deficient Glycoprotein SYNNational Human Genome Research Institute1997–1999
