pseudosyringomyelic syndrome
偽脊髄空洞症性症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
English Journal
- Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease.
- Zyss J1, Béhin A, Couvert P, Bouhour F, Sassolas A, Kolev I, Denys V, Vial C, Lacour A, Carrié A, Stojkovic T.
- Journal of neurology.J Neurol.2012 Jun;259(6):1222-6. doi: 10.1007/s00415-011-6340-2. Epub 2011 Dec 17.
- Tangier disease (TD) (OMIM#205400) is a rare autosomal recessive disorder resulting from mutations in the ABCA1 gene, leading to decreased levels of plasma high-density lipoproteins (HDL). Peripheral neuropathy is a common finding in this disease, and may present as relapsing/remitting mono/polyneur
- PMID 22179783
- [Pathologic cataract in pseudosyringomyelic ulceromutilating acropathy].
- Vilă F.
- Revista de chirurgie, oncologie, radiologie, o. r. l., oftalmologie, stomatologie. Seria: Oftalmologie.Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Oftalmol.1988 Jul-Sep;32(3):207-10.
- PMID 2973635
- [A typical history of non-familial pseudosyringomyelic acropathy of the lower extremity (Bureau-Barriere syndrome)].
- MILLERET P, GONDY B.
- Journal de médecine de Lyon.J Med Lyon.1960 Apr 20;41:421-6.
- PMID 14422589
Related Pictures
★リンクテーブル★
[★]
- 英
- pseudosyringomyelic syndrome
[★]