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Long -term Biochemical Results after Operative Treatment of Primary Hyperparathyroidism Associated with Multiple Endocrine Neoplasia Types I and Ila: Is a More or Less Extended Operation Essential.
Acromegaly caused by growth hormone-relating hormone in a patient with multiple endocrine neoplasia type I.
Familial cutaneous lichen amyloidosis in association with multiple endocrine neoplasia type 2A: a new variant.
Key Words: bowel obstruction, intestinal neuroma, multiple endocrine neoplasia type 2.
7] Human genes: MEN1, multiple endocrine neoplasia 1; RET, ret protooncogene (multiple endocrine neoplasia and medullary thyroid carcinoma 1, Hirschsprung disease).
4) Multiple endocrine neoplasia type 1 (MEN-1) is also seen in 25% of patients with thymic carcinoid.
Patients may have a history of neck irradiation, a family history of multiple endocrine neoplasia, familial hyperparathyroidism, or familial hyperparathyroidism with a jaw tumor; the latter is suggestive of parathyroid cancer.
2), (8) Multiple endocrine neoplasia Type I is present in 7.
DIAGNOSIS: Multiple endocrine neoplasia (MEN), type 1.
is contraindicated in patients with a personal or family history of MTC and in patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
Pancreatic endocrine neoplasms are usually sporadic but may be part of hereditary syndromes mostly including multiple endocrine neoplasia type 1 (MEN-1) and, more rarely, von Hippel-Lindau (VHL) syndrome, neurofibromatosis type 1 (NF1), and tuberous sclerosis complex (TSC).
In 2 of these 14 cases, multiple endocrine neoplasia was subsequently diagnosed.

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