Dr. Eniko K Pivnick MD
Geneticist | Clinical Genetics (M.D.)
51 N DUNLAP ST STE 400 MEMPHIS TN, 38105About
Dr. Eniko Pivnick practices Genetic Medicine in Memphis, TN. As a geneticist, Dr. Pivnick performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Pivnick carries out studies, tests, and counsels patients with genetic diseases.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1.
- Long-term survival in Patau syndrome.
- Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis.
- Treatment of diffuse basal cell carcinomas and basaloid follicular hamartomas in nevoid basal cell carcinoma syndrome by wide-area 5-aminolevulinic acid photodynamic therapy.
- An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea.
- Wilms tumor in a patient with 22q11.2 microdeletion.
- Trigeminal nerve agenesis with absence of foramina rotunda in Gómez-López-Hernández syndrome.
- Neonatal Hospital Course and Outcomes of Live-born Infants with Trisomy 18 at Two Tertiary Care Centers in the United States.
- Rickets secondary to phosphate depletion. A sequela of antacid use in infancy.
- A jumping Robertsonian translocation: a molecular and cytogenetic study.
- Bony orbital morphology in neurofibromatosis type 1 (NF1).
- Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients.
- Infant with midline thoracoabdominal schisis and limb defects.
- Alternative splicing of exons 29 and 30 in the neurofibromatosis type 1 gene.
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