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References in periodicals archive ?
C-cell hyperplasia (CCH) in a patient with multiple endocrine neoplasia 2A.
Pheochromocytoma has long been estimated to be hereditary in 10-15% of cases and may occur as part of Von Hippel-Lindau disease (VHL Gene), MEN (Multiple Endocrine Neoplasia) Syndrome Type IIA (medullary carcinoma of thyroid, pheochromocytoma, and parathyroid adenoma) (RET gene) or MEN IIB (medullary carcinoma of thyroid, Pheochromocytoma, Marfan's and neurofibromatosis) (NF1 gene).
Insulinomas in multiple endocrine neoplasia type 1.
Turner, "Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1," Archives of Dermatology, vol.
Linear cutaneous neuromas (dermatoneurie en stries): a limited phakomatosis with striated pigmentation corresponding to cutaneous hyperneury (featuring multiple endocrine neoplasia syndrome?).
* Inherited diseases associated with secondary hypertension include polycystic kidney disease, multiple endocrine neoplasia type 2 (MEN2), and von Hippel-Lindau syndrome.
Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene.
These include Turner syndrome (50%), Addison's disease (20%), Down's syndrome (20%), multiple endocrine neoplasia II (70%), and POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes) (50 %).
E, an endocrinologist, diagnosed a patient with multiple endocrine neoplasia type I, a rare disorder that is inherited in an autosomal dominant fashion.
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