Síndrome de Gardner: Rara variedad con fibromatosis mesentérica

Alfonso Hernández, Lorenzo I; Fleites Batista, Gilberto; Más Navarro, Orlando; Barthelemy, Guillermo.
Rev. cuba. cir ; 7(4-5-6): 463-71, dic.-31-1968. ilus
Artículo en Español | CUMED | ID: cum-10964

Documentos relacionados

  1. Superficial fibromas with CTNNB1 mutation.
  2. Giant mesenteric fibromatosis associated with non-Hodgkin lymphoma. A case report and literature review.
  3. Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis.
  4. Adipocyte-rich <i>CTNNB1</i>-mutated Intramuscular Gardner Fibroma Progressing to Desmoid Fibromatosis.
  5. Atypical Gardner's Syndrome with Proptosis as the Primary Symptom.
  6. Mesenteric fibromatosis. Case report.
  7. [Gardner syndrome with chronic osteomyelitis of the jaw: a case report].
  8. Incomplete Gardner's syndrome with blepharoptosis as the first symptom.
  9. [Gardner's syndrome, a rare disease].
  10. The challenge of extraabdominal desmoid tumour management in patients with Gardner's syndrome: radiofrequency ablation, a promising option.