نتایج جستجو برای: von recklinghausen
تعداد نتایج: 96693 فیلتر نتایج به سال:
Neurofibromatosis type 1, also called Von Recklinghausen Disease is a genetic disorder characterized by the development of multiple benign tumors affecting skin and nervous system. It disease with prevalence one case in 3000 births. The cause VRD mutation [1-4]. In half all cases NF1, faulty gene passed from parent to their child. Clitoromegaly presenting childhood can be congenital or acquired...
Von Recklinghausen described the features of multiple neurofibromatosis in 1882, though Willis (1962) points out that there had been several earlier descriptions of the condition including a monograph by Smith (1849). Brooks and Lehman (1924) drew attention to the skeletal abnormalities in this condition. Crowe, Schull, and Neel (1956) made a clinical, pathological, and genetic study of 223 cas...
Neurofibromatosis type 1 (NF-1) is an autosomal dominant neurocutaneous syndrome which is characterized by formation of neurofibromas all over the skin and various other body systems. The anaesthetic management of these patients requires attention to all possible abnormalities and associated disturbances to prevent any peri-operative complication. NF-1-associated complications of the musculoske...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal dominant disorder characterized by abnormalities in multiple tissues derived from the embryonic neural crest. Portions of the gene have been recently identified by positional cloning, and sequence analysis has shown homology to the GTPase activating protein (GAP) family. In this report we present the ...
Résumé La neurofibromatose de type 1 (NF1) ou maladie de Von Recklinghausen est une maladie héréditaire la plus fréquente des phacomatoses, de transmission autosomique dominante. Ses complications pulmonaires sont rarement décrites dans la littérature. Les complications vasculaires sont retrouvées chez 3,6% des patients. Nous rapportons le cas d'une patiente âgée de 38 ans, suivie pour neurofib...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید