Familial endocrine neoplasia type I

Introduction: Familial endocrine neoplasia type I

Description of Familial endocrine neoplasia type I

Familial endocrine neoplasia type I (medical condition): Rare inherited disease causing tumors in multiple glands. See also Multiple endocrine neoplasia type 1:
  »Introduction: Multiple endocrine neoplasia type 1
  »Symptoms of Multiple endocrine neoplasia type 1

Familial endocrine neoplasia type I as a Disease

Familial endocrine neoplasia type I: Another name for Multiple endocrine neoplasia type 1 (or close medical condition association).
  »Introduction: Multiple endocrine neoplasia type 1
  »Symptoms of Multiple endocrine neoplasia type 1

Familial endocrine neoplasia type I: Familial endocrine neoplasia type I is listed as a type of (or associated with) the following medical conditions in our database: Multiple endocrine neoplasia, Pituitary conditions, Pancreas conditions, Genetic Disease

Symptoms of Familial endocrine neoplasia type I (Multiple endocrine neoplasia type 1)

Some of the symptoms of Familial endocrine neoplasia type I incude:

• Abdominal pain
• Abdominal distension
• Anorexia
• Nausea
• Polyuria

See full list of 51 symptoms of Familial endocrine neoplasia type I (Multiple endocrine neoplasia type 1)

Familial endocrine neoplasia type I: Article Excerpts about Multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 (MEN1) is an inherited disorder that affects the endocrine glands. It is sometimes called multiple endocrine adenomatosis or Wermer's syndrome, after one of the first doctors to recognize it. (Source: excerpt from Multiple Endocrine Neoplasia Type 1: NIDDK)

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