phenytoin has been researched along with Hamartoma Syndrome, Multiple in 1 studies
Hamartoma Syndrome, Multiple: A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.
Excerpt | Relevance | Reference |
---|---|---|
"In this study brain tumors developing with tuberous sclerosis were biologically benign; total transcortical tumor removal permanently relieved the attending cerebral hypertension and achieved prolonged survival without notable functional impairment." | 2.35 | Brain tumors in hereditary multiple system hamartomatosis (tuberous sclerosis). ( Cooper, JR, 1971) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cooper, JR | 1 |
1 review available for phenytoin and Hamartoma Syndrome, Multiple
Article | Year |
---|---|
Brain tumors in hereditary multiple system hamartomatosis (tuberous sclerosis).
Topics: Anticonvulsants; Astrocytoma; Brain Neoplasms; Cerebral Ventricles; Child; Diagnosis, Differential; | 1971 |