Dr. Sancy A Leachman M.D.
Dermatologist | Procedural Dermatology
50 N Medical Dr Salt Lake City UT, 84132About
Dr. Sancy Leachman is a dermatologist practicing in Salt Lake City, UT. Dr. Leachman specializes in skin care. Dermatologists evaluate and manage both common and uncommon skin conditions. These conditions include acne, psoriasis, warts, skin infections, atopic dermatitis, herpes simplex and more. Dermatologists are also experts in more complex skin diseases like impetigo, hidradenitis and milaria. Dr. Leachman diagnoses skin problems and develops unique treatments plans for each individual patient.
Board Certification
DermatologyAmerican Board of DermatologyABD
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Preservation of RNA for functional genomic studies: a multidisciplinary tumor bank protocol.
- Failure to detect differences in proliferation status of nevi from CDKN2A mutation carriers and non-carriers.
- Ubiquitin-fused and/or multiple early genes from cottontail rabbit papillomavirus as DNA vaccines.
- A giant verruciform xanthoma.
- Metastatic melanoma in pregnancy: risk of transplacental metastases in the infant.
- Pancreatic carcinoma surveillance in patients with familial melanoma.
- Novel application of a fibrin cell block method to evaluate melanocytic cell populations.
- Vulvar melanoma: diffuse melanosis and metastasis to the placenta.
- Clinical germline genetic testing for melanoma.
- Accumulation, activation and interindividual variation of the epidermal TP53 protein in response to ionizing radiation in organ cultured human skin.
- Proliferative nodules in congenital melanocytic nevi: a clinicopathologic and immunohistochemical analysis.
- Longitudinal assessment of the nevus phenotype in a melanoma kindred.
- Motivating factors for attendance of skin cancer screenings.
- Evaluation of a 7-day continuous intravenous infusion of decitabine: inhibition of promoter-specific and global genomic DNA methylation.
- Melanoma cells express elevated levels of phosphorylated histone H2AX foci.
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