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[The Wermer syndrome]

E Târcoveanu1, V Strat, E Cotea

  • 1Clinica I Chirurgie, Spitalul Universitar Sf. Spiridon, Iaşi.

Chirurgia (Bucharest, Romania : 1990)
|July 1, 1997
PubMed
Summary
This summary is machine-generated.

Managing gastrinoma in patients with Multiple Endocrine Neoplasia type I (MEN I) is challenging. This study reviews literature and presents two cases of Wermer syndrome, highlighting diagnostic and therapeutic complexities.

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Area of Science:

  • Endocrinology
  • Genetics
  • Oncology

Background:

  • Multiple Endocrine Neoplasia type I (MEN I), also known as Wermer syndrome, is a rare genetic disorder.
  • It is typically inherited in an autosomal dominant pattern with variable penetrance.
  • MEN I is characterized by tumors in the parathyroid glands, pituitary (adenohypophyseal) cells, and pancreatic islets.