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Related to neurofibromatosis: Neurofibromatosis Type 2, Neurofibromatosis Type 1
References in periodicals archive ?
The group is intended to enable neurofibromatosis patients and their families to connect and talk about the condition and to challenge the stigma that sufferers face.
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.
Schwanomas representan el 8% de los tumores intracraneales, 85% de los tumores del angulo pontocerebeloso y 29% de los tumores de las raices nerviosas espinales; 90% son unicos; y tan solo 10% son multiples se encuentran asociados a neurofibromatosis tipo 2 el 4%1 (1,2,3,4); el pico de incidencia en los Shcwanomas vestibulares se encuentra entre la cuarta y sexta decada de la vida, sin embargo, en el caso de los Schwannomas bilaterales su presentacion es 14 anos antes en promedio a la edad de 25 anos; aunque pueden presentarse a cualquier edad (1,4,5,6).
Von Recklinghausen neurofibromatosis a clinical and population study in south-east wales.
These cases account for about one half of neurofibromatosis.
Gupta, "Rib head protrusion into the central canal in type 1 neurofibromatosis," Pediatric Radiology, vol.
On the other hand, neurofibromatosis (NF) is a common genodermatosis of autosomal dominant variant with an incidence of 1 in 3000 births.
1,15) Neurofibromatosis Type 2 is diagnosed on the basis of a series of clinical criteria, defined by the presence of bilateral vestibular schwannomas leading to hearing loss, (5) cataracts, and central nervous system involvement, such as meningioma.
People who commune along persons with Neurofibromatosis do not have to worry that they will acquire the disease as well.
Our case highlights an atypical presentation of pheochromocytoma in a patient with Neurofibromatosis type 1 who developed cardiogenic shock with multi-organ failure.