耳口蓋指趾症候群
WordNet
- relating to or performed with the fingers; "digital examination"
- displaying numbers rather than scale positions; "digital clock"; "digital readout"
- of a circuit or device that represents magnitudes in digits; "digital computer"
- one of the elements that collectively form a system of numeration; "0 and 1 are digits" (同)figure
- a finger or toe in human beings or corresponding body part in other vertebrates (同)dactyl
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- a dialect of the Chiwere language spoken by the Oto (同)Otoe
- a member of the Siouan people inhabiting the valleys of the Platte and Missouri rivers in Nebraska (同)Otoe
PrepTutorEJDIC
- 指の / 数字の;計数型の / (タイプライターなどの)鍵(けん),キー
- (手足の)指 / アラビア数字(0から9までの一つ;0を除くこともある)
- (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
UpToDate Contents
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English Journal
- Bifid tongue, corneal clouding, and Dandy-Walker malformation in a male infant with otopalatodigital syndrome type 2.
- Murphy-Ryan M, Babovic-Vuksanovic D, Lindor N.SourceMayo Medical School, Rochester, Minnesota, USA.
- American journal of medical genetics. Part A.Am J Med Genet A.2011 Apr;155A(4):855-9. doi: 10.1002/ajmg.a.33901. Epub 2011 Mar 15.
- We report on a male infant with otopalatodigital syndrome type 2 (OPD2) associated with a novel c.514C>G FLNA mutation and unusual clinical features including bifid tongue and congenital corneal clouding. Bifid tongue and congenital corneal clouding have each only been described once previously i
- PMID 21412975
- Omphalocele and gastroschisis and associated malformations.
- Stoll C, Alembik Y, Dott B, Roth MP.SourceGénétique Médicale, Faculté de Medecine, Strasbourg, France. claude.stoll@medecine.u-strasbg.fr
- American journal of medical genetics. Part A.Am J Med Genet A.2008 May 15;146A(10):1280-5. doi: 10.1002/ajmg.a.32297.
- The etiology of gastroschisis and omphalocele is unclear and their pathogenesis is controversial. Because previous reports have inconsistently noted the type and frequency of malformations associated with omphalocele and gastroschisis, we assessed these associated malformations ascertained between 1
- PMID 18386803
Japanese Journal
- A Japanese case of oto-palato-digital syndrome type 2: an apparent lack of phenotype-genotype correlation
- Pierre Robin sequence を伴った1型耳・口蓋・指症候群の兄弟例
- oto-palato-digital syndrome の兄弟例
Related Links
- Otopalatodigital syndrome type 2 is a disorder involving abnormalities in skeletal development and other health problems. It is a member of a group of related conditions called otopalatodigital spectrum disorders, which ...
- More Oto-Palato-digital syndrome type 1 animations & videos Oto-Palato-digital syndrome type 1: Broader Related Topics Congenital conditions - physical defects Congenital conditions Head conditions Oral conditions Bone or ...
★リンクテーブル★
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- 英
- Taybi syndrome
- 同
- 耳口蓋指症候群 oto-palate-digital症候群 otopalatodigital syndrome oto-palato-digital syndrome OPD syndrome
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- 関
- digitus、finger、numeral、order、order of magnitude
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- 関
- quantal
- 直腸診の略
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