WordNet
- the means of connection between things linked in series (同)nexus
- a unit of length equal to 1/100 of a chain
- an interconnecting circuit between two or more locations for the purpose of transmitting and receiving data (同)data link
- a fastener that serves to join or connect; "the walls are held together with metal links placed in the wet mortar during construction" (同)linkup, tie, tie-in
- (computing) an instruction that connects one part of a program or an element on a list to another program or list
- of or relating to the mind; "mental powers"; "mental development"; "mental hygiene"
- affected by a disorder of the mind; "a mental patient"; "mental illness"
- involving the mind or an intellectual process; "mental images of happy times"; "mental calculations"; "in a terrible mental state"; "mental suffering"; "free from mental defects"
- of or relating to the chin- or liplike structure in insects and certain mollusks
- the extent to which something is delayed or held back
- lack of normal development of intellectual capacities (同)mental_retardation, backwardness, slowness, subnormality
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- the 24th letter of the Roman alphabet (同)x, ex
PrepTutorEJDIC
- (鎖の)『輪』,環 / 鎖のようにつながったソーセージの一節 / (…と)つなぐ物(人),(…との)きずな,つながり《+『with』(『to』)+『名』》 / 《複数形で》=cuff links / …‘を'『つなぎ合わせる』,連結する;(…と)…‘を'つなぐ《+『名』+『with』(『to』)+『名』》 / (…と)結合する,つながる《+[『up』(『together』)]『with』+『名』》
- たいまつ
- 『精神の』,心の / 頭脳の,知能の / 《名詞の前にのみ用いて》精神病の / 《名詞の前にのみ用いて》頭の中で行う / 《英話》《補語にのみ用いて》頭のおかしい,気がふれた
- 〈U〉遅延,遅滞 / 〈C〉遅らせるもの;妨害物 / 〈U〉〈C〉知能(学業など)の遅れ
- (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
- Christ / Christian
UpToDate Contents
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- 1. Primary care of the adult with intellectual disability (mental retardation)
- 2. Intellectual disability in children: Evaluation for a cause
- 3. ペリツェウス・メルツバッハー病 pelizaeus merzbacher disease
- 4. カウデン症候群などのPTEN過誤腫症候群 pten hamartoma tumor syndrome including cowden syndrome
- 5. Intellectual disability in children: Definition, diagnosis, and assessment of needs
English Journal
- Distal Xq28 microdeletions: Clarification of the spectrum of contiguous gene deletions involving ABCD1, BCAP31, and SLC6A8 with a new case and review of the literature.
- Calhoun AR1, Raymond GV.
- American journal of medical genetics. Part A.Am J Med Genet A.2014 Oct;164(10):2613-7. doi: 10.1002/ajmg.a.36661. Epub 2014 Jul 9.
- The contiguous ABCD1/DXS1375E (BCAP31) deletion syndrome (CADDS) is a rare X-linked contiguous gene deletion syndrome with a severe clinical phenotype that includes marked delays, significant growth failure, liver dysfunction, and early death. The X-linked creatine transporter deficiency is a consid
- PMID 25044748
- A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism.
- De Wolf V1, Crepel A, Schuit F, van Lommel L, Ceulemans B, Steyaert J, Seuntjens E, Peeters H, Devriendt K.
- American journal of medical genetics. Part A.Am J Med Genet A.2014 Sep 24. doi: 10.1002/ajmg.a.36752. [Epub ahead of print]
- We present a male patient with sporadic Aarskog syndrome, cleft palate, mild intellectual disability, and autism spectrum disorder (ASD). A submicroscopic discontiguous deletion was detected on chromosome Xp11.2 encompassing FGD1, FAM120C, and PHF8. That the deletion encompassed FGD1 (exons 2-8) exp
- PMID 25258334
- Leiomyosarcoma With Alternative Lengthening of Telomeres Is Associated With Aggressive Histologic Features, Loss of ATRX Expression, and Poor Clinical Outcome.
- Liau JY1, Tsai JH, Jeng YM, Lee JC, Hsu HH, Yang CY.
- The American journal of surgical pathology.Am J Surg Pathol.2014 Sep 16. [Epub ahead of print]
- Leiomyosarcoma is an aggressive soft tissue sarcoma with poor patient survival. Recently, it was shown that 53% to 62% of leiomyosarcomas use the alternative lengthening of telomeres (ALT) as their telomere maintenance mechanism. The molecular basis of this mechanism has not been elucidated. Studies
- PMID 25229770
Japanese Journal
- 重度精神遅滞と難治てんかんを呈したMECP2重複症候群の2男児例
- 齋藤 貴志,本田 尚三,中川 栄二,花井 彩江,小牧 宏文,須貝 研司,佐々木 征行,赤坂 紀幸,遠山 潤,稲澤 譲治,後藤 雄一
- てんかん研究 28(1), 24-31, 2010
- … 両症例ともX染色体全領域のアレイcomparative genomic hybridizationの結果、MECP2 を含むXq28の重複がみられた。 … MECP2 の重複患者は、X連鎖性精神遅滞の1％を占めるといわれている。 …
- NAID 130000303469
- X連鎖αサラセミア・精神遅滞症候群(ATR-X症候群)
- 和田 敬仁
- 臨床病理 57(4), 382-390, 2009-04-25
- NAID 10025224846
Related Links
- Schimke, X-linked, mental retardation syndrome: Introduction Schimke, X-linked, mental retardation syndrome: A very rare syndrome characterized by mental retardation, abnormal involuntary movements and retarded growth. More ...
- Wilson-Turner syndrome Wilson-Turner syndrome An extremely rare (14 cases in the world literature, in a single cohort) X-linked condition (OMIM:309585) condition characterised by obesity, gynaecomastia, speech difficulties ...
Related Pictures
★リンクテーブル★
| リンク元 | 「X連鎖性精神遅滞症候群」「X-linked mental retardation」「X連鎖精神遅滞症候群」 |
| 関連記事 | 「link」「mental」「retardation」「linked」「X」 |
「X連鎖性精神遅滞症候群」
「X-linked mental retardation」
「X連鎖精神遅滞症候群」
「link」
- n.
- v.
- 関連づける、連結する、連接する
- 関
- associate、association、attach、bearing、bind、catenate、catenation、concatenation、connect、connection、correlate、correlation、implicate、implication、join、juncture、ligate、ligation、linkage、linked、pertinent、reference、relate、relation、relationship、relative、relevance、relevant
「mental」
- adj.
- 精神的な、心理の
「retardation」
- n.
- 遅延、遅滞
- 関
- (adj.)retard
- 関
- deceleration、delay、[[]]
「linked」
- adj.
- 連鎖の、連鎖的な、連鎖性の