| 单词 | neurofibromatosis type 1 | 
| 释义 | > as lemmasneurofibromatosis type 1   Originally (now also  neurofibromatosis type 1): an inherited (autosomal dominant) disorder characterized by the development of multiple neurofibromas, esp. in the dermis and subcutaneous tissue, with areas of hyperpigmentation of the skin (also called von Recklinghausen's disease). Later also (chiefly with distinguishing word): any of several other inherited conditions characterized by multiple nerve sheath tumours; esp. (more fully  central neurofibromatosis,  neurofibromatosis type 2) an autosomal dominant disorder in which there is predisposition to bilateral acoustic schwannomas and other benign tumours of the central nervous system. ΘΚΠ the world > health and disease > ill health > a disease > disorders of internal organs > disorders of nervous system > 			[noun]		 > nerve tumour neuroma1829 neurofibroma1887 neurofibromatosis1896 neurinoma1913 neurilemoma1935 1896    Brit. Med. Jrnl. 10 Oct. 1024/1 		(heading)	  				On neuro-fibromatosis and tumours relating to nerves. 1899    Lancet 29 July 271/2  				The nature of Recklinghausen's disease or, as it has sometimes been called, generalised neuro-fibromatosis. 1949    H. W. C. Vines Green's Man. Pathol. 		(ed. 17)	 xxxix. 1172  				Multiple neurofibromatosis or von Recklinghausen's disease is a rare familial disease in which there may be very numerous subcutaneous neurofibromata all over the body. 1973    Daily Colonist 		(Victoria, Brit. Columbia)	 4 Oct. 2/3  				A rare condition called neurofibromatosis is featured by multiple bumps. 1989    New Scientist 10 June 31/3  				The result of this loss is the array of grotesque but non-malignant tumours that characterise neurofibromatosis. 1991    Ann. Otol., Rhinol. & Laryngol. 100 38  				The neurofibromatoses are two distinct entities with different genetic origins. 1994    W. Maples  & M. Browning Dead Men do tell Tales viii. 113  				Dr. Frederick Treves, who discovered the Elephant Man and wrote the original monograph on him, diagnosed Merrick as suffering from multiple neurofibromatosis. But recent articles have suggested that it might be Proteus syndrome. 2000    Angiology 51 733  				Neurofibromatosis regroups at least two different autosomal dominant genetic disorders: neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2). < as lemmas | 
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