Your browser doesn't support javascript.
loading
Prothrombin Gene Mutation as a Teaching Tool: An Autobiographical Case Report.
Morris, Tucker; Lorbeer, Elizabeth R; Roach, Richard R.
Afiliación
  • Morris T; Department of Medical Education, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, USA.
  • Lorbeer ER; Department of Medical Library, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, USA.
  • Roach RR; Department of Internal Medicine, Western Michigan University Homer Stryker M.D. School of Medicine, Kalamazoo, USA.
Cureus ; 15(1): e33967, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36820119
ABSTRACT
The prothrombin G20210A factor II mutation carrier status has been reported to cause complications during pregnancy. This report presents the case of a patient diagnosed with heterozygous prothrombin G20210A factor II mutation at 29 years of age during preconception genetic screening. The patient had two uncomplicated pregnancies. The patient underwent laparoscopic cholecystectomy with a complicated postoperative course. The complications included deep vein thrombophlebitis (DVT), portal vein thrombosis (PVT), and pulmonary embolization (PE). The treatment options and contraceptive choices are also discussed in this report. Our report discusses the subsequent risks inherent in a heterozygote following the administration of oral contraceptives, prolonged immobilization related to lower extremity trauma, and extended motor vehicle excursion.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Cureus Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Cureus Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos