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.
Molecular genetics of
multiple endocrine neoplasia types 1 and 2.
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.
Quality of Life in Patients with
Multiple Endocrine Neoplasia Types I.