オピッツ症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- of or relating to or situated in the larynx; "laryngeal infection"
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
- 喉頭(こうとう)の;(音声が)喉頭音の
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adult.
- de Silva D1, Osborne A, Simpson SA, Dean JC, Seaton A.
- Thorax.Thorax.1998 Feb;53(2):149-50; discussion 148.
- PMID 9624301
Related Links
- Opitz syndrome is caused by an inherited, genetic defect. There are two forms of inheritance for Opitz syndrome. One is autosomal dominant, meaning that the gene only has to be passed on from one parent for a child to have the ...
- Thorax 1998;53:149–150 149 Opitz oculo-genito-also suggested that this condition should be included in the diVerential diagnosis of laryngeal syndrome: a recurrent aspiration pneumonia. (Thorax 1998;53:149–150) rare cause of ...
★リンクテーブル★
[★]
- 英
- Opitz syndrome
- 同
- オピッツ・フリアス症候群 Opitz-Frias syndrome、両眼開離尿道下裂症 telecanthus hypospadias、Opitz oculo-genito-laryngeal syndrome
- Opitz syndrome , Opitz-Frias syndrome a familial syndrome consisting of hypertelorism and hernias, and in males also characterized by hypospadias, cryptorchidism, and bifid scrotum. Cardiac, laryngotracheal, pulmonary, anal, and renal abnormalities may also be present.
[★]
- 関
- larynx
[★]