Terms: = Ovarian cancer AND PTCH1, RP11-435O5_3, Q13635, PTCH, 5727, HPE7, FLJ26746, NBCCS, BCNS, PTC1, ENSG00000185920, FLJ42602 AND Diagnosis
10 results:
1. Bilateral ovarian fibromas as the sole manifestation of Gorlin syndrome in a 22-year-old woman: a case report and literature review.
Zhu M; Li J; Duan J; Yang J; Gu W; Jiang W
Diagn Pathol; 2023 Oct; 18(1):118. PubMed ID: 37907964
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2. Case report of bilateral ovarian fibromas associated with de novo germline variants in ptch1 and SMARCA4.
Higashimoto T; Smith CH; Hopkins MR; Gross J; Xing D; Lee JW; Morris T; Bodurtha J
Mol Genet Genomic Med; 2022 Sep; 10(9):e2005. PubMed ID: 35775118
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3. ptch1-GLI1 Fusion-Positive ovarian Tumor: Report of a Unique Case With Response to Tyrosine Kinase Inhibitor Pazopanib.
Alwaqfi RR; Samuelson MI; Guseva NN; Ouyang M; Bossler AD; Ma D
J Natl Compr Canc Netw; 2021 Sep; 19(9):998-1004. PubMed ID: 34551385
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4. Hereditary non-BRCA gynecological tumors.
Vellone VG; Paudice M; Varesco L
Minerva Ginecol; 2016 Oct; 68(5):579-86. PubMed ID: 26930387
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5. Gorlin syndrome with an ovarian leiomyoma associated with a ptch1 second hit.
Akizawa Y; Miyashita T; Sasaki R; Nagata R; Aoki R; Ishitani K; Nagashima Y; Matsui H; Saito K
Am J Med Genet A; 2016 Apr; 170A(4):1029-34. PubMed ID: 26782978
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6. [Gorlin syndrome in the paediatric age].
Roncalés-Samanes P; Peña-Segura JL; Fernando-Martínez R; Fuertes-Rodrigo C; García-Oguiza A; López-Pisón J
Rev Neurol; 2014 Apr; 58(7):303-7. PubMed ID: 24677153
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7. Nevoid basal cell carcinoma syndrome with a unilateral giant ovarian fibroma in a Japanese 6-year-old girl.
Jimbo T; Masumoto K; Urita Y; Takayasu H; Shinkai T; Uesugi T; Gotoh C; Sakamoto N; Sasaki T; Oto T; Fukushima T; Noguchi E; Nakano Y
Eur J Pediatr; 2014 May; 173(5):667-70. PubMed ID: 24257914
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8. Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland.
Steffen J; Nowakowska D; Niwińska A; Czapczak D; Kluska A; Piatkowska M; Wiśniewska A; Paszko Z
Int J Cancer; 2006 Jul; 119(2):472-5. PubMed ID: 16770759
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9. Gorlin syndrome presenting as prenatal chylothorax in a girl.
Geneviève D; Walter E; Gorry P; Jacquemont ML; Dupic L; Layet V; Munnich A; Cormier-Daire V; Dommergues M; Lyonnet S; Mitanchez D
Prenat Diagn; 2005 Nov; 25(11):997-9. PubMed ID: 16231297
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10. Radiological features in 82 patients with nevoid basal cell carcinoma (NBCC or Gorlin) syndrome.
Kimonis VE; Mehta SG; Digiovanna JJ; Bale SJ; Pastakia B
Genet Med; 2004; 6(6):495-502. PubMed ID: 15545745
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