microcephaly，英語單詞，主要用作名詞，作名詞時譯為“頭小畸型（複數microcephalies，形容詞microcephalic）”。
頭圍較正常小兒低於2個標準差（S.D）以上時，將其診斷為頭小畸形（microcephaly）。引起頭小畸形的原因很多，母妊娠早期各種有害因素（感染、營養不良、中毒、放射線）均有可能影響胎兒顱腦的發育。代謝異常、染色體畸變（如21三體、18三體、13三體或其他異常）也常合併頭小畸形，還有一些家族遺傳性頭小畸形。出生時...
（microcephaly） 原發性者常染色體隱性遺傳所致，繼發性者因孕婦病毒感染或其他原因所致。前者多伴有中、重度智力低下，後者的智力水平視病因及頭小的程度而定。腦回畸形 （gyrus deformation） 包括無腦回， 腦 回大或小等畸形、均有明顯的智力及情緒障礙。精神障礙 兒童精神分裂症 （childhood schizophrenia） 兒童...
小頭[畸形]小頭[畸形]（microcephaly）是1995年公布的醫學名詞。公布時間 1995年，經全國科學技術名詞審定委員會審定發布。出處 《醫學名詞 第三分冊》。
* 小腦症（Microcephaly）* 韋二氏綜合徵（Muckle-Wells Syndrome）* 非綜合徵型耳聾（Nonsyndromic deafness）* Nonsyndromic deafness, autosomal dominant * Nonsyndromic deafness, autosomal recessive * 帕金森氏症 * 嗜鉻細胞瘤（Pheochromocytoma）* 紫質症（porphyria）* 遲發性皮膚卟啉症（porphyria cutanea tarda）...
還有其他數個與此症相關的特徵如唇顎裂(cleftlipandpalate)、氣管-食道廔管或閉鎖(tracheo-esophagealfistulaoratresia)、顏面麻痹(facialpalsy)、吞嚥的問題(swallowingproblems)、身體抵抗力較差(weakupperbodystrength)、癲癇(seizures)、小頭畸型(microcephaly)、腦下垂體異常(abnormalitiesofthepituitarygland)以及較差的...
顏面的火焰狀母斑：伯-韋綜合徵，即臍膨出-巨舌-巨大軀體綜合徵，亦稱EMG綜合徵、WiedemannⅡ型綜合徵、Wilm瘤和半身肥大綜合徵、Beckwith綜合徵、新生兒低血糖巨內臟巨舌小頭綜合徵(neonatalhypoglycemiavisceromegalymacroglossiamicrocephalysyndrome)等。據統計，低血糖的發生率約占33%～50%。內臟肥大也常見，如肝、腎...
the brain. Affected individuals generally have seizures beginning in the first few months of life. Babies with GLUT1 deficiency syndrome have a normal head size at birth, but growth of the brain and skull is often slow, in severe cases resulting in an abnormally small head size(microcephaly)....
伯-韋綜合徵(Beckwith-Wiedemann syndrome)即突臍、巨舌、巨體綜合徵(exomphalos-macroglossia-gigantism syndrome) ， 亦稱EMG 綜合徵、WiedemannⅡ型綜合徵、Wilm 瘤和半身肥大綜合徵、Beckwith 綜合徵、新生兒低血糖巨內臟巨舌小頭綜合徵(neonatal hypoglycemia visceromegaly macroglossia microcephaly syndrome)等。疾病...
megacephaly，英語單詞，主要用作為名詞，用作名詞譯為“巨頭，巨頭畸形”。單詞用法 N the condition of having an unusually large head or cranial capacity. It can be of congenital origin or result from an abnormal overgrowth of the facial bones 巨頭症 → compare microcephaly 網路釋義 巨頭 ...
小頭畸形(microcephaly)先天性腦積水(congenitalhydrocephalus)中腦導水管畸形(malformationsofaqueductofsylvius)第四腦室正中孔和外側孔閉鎖(atresiaofforaminaofMagendieandLuschka)胼胝體發育不全(agenesisofcorpuscallosum)前腑無裂征(holoprosencephaly)3第三章眼、耳、面和頸部先天性畸形 無眼(anophthalmos)小眼(microph...
另一方面，中心體蛋白的突變能引起許多人類遺傳病，包括小腦畸形 (microcephaly)和一系列纖毛病 (ciliopathies)，後者嚴重影響神經、腎臟、肝臟、視覺等器官的發育。我們將結合超高解析度顯微技術、生化手段、哺乳動物細胞和果蠅遺傳學等，研究中心體在細胞對稱或不對稱分裂、細胞分化過程中的動態變化以及功能，進而研究在...
[醫] 巨頭 medionecrosis 主動脈中層壞死 megalocephaly 巨頭 megalocytosis 巨紅細胞症 單詞用法 1.N the condition of having an unusually large head or cranial capacity. It can be of congenital origin or result from an abnormal overgrowth of the facial bones 巨頭症 → compare microcephaly ...
伯-韋綜合徵(Beckwith-Wiedemannsyndrome)即臍膨出-巨舌-巨大軀體綜合徵(exomphalos-macroglossia-gigantismsyndrome)，亦稱EMG綜合徵、WiedemannⅡ型綜合徵、Wilm瘤和半身肥大綜合徵、Beckwith綜合徵、新生兒低血糖巨內臟巨舌小頭綜合徵(neonatalhypoglycemiavisceromegalymacroglossiamicrocephalysyndrome)等。據統計，低血糖的...
CongenitalCerebellar HypoplasiaRhombencephalosynapsisCongenital Vermian HypoplasiaDandy-Walker SpectrumAtretic Parietal CephaloceleCallosal DysgenesisHoloprosencephalySeptooptic DysplasiaKallman SyndromePituitary Stalk AnomaliesHamartoma of Tuber CinereumMicrocephalyHemimegalencephalySchizencephalyClassial LissencephalyCongenital ...
(4) 我們同時也在做先天性小腦病(PRIMARY MICROCEPHALY)基因之一MCPH1 (MICROCEPHALIN) 的功能性研究。先天性小頭畸形是一種罕見的神經疾病，這種疾病是由於大腦的形成和生長不正常而導致患者頭部異常小。患這種疾病的兒童可能很矮小並且伴有癲癇發作，而且出現一定程度的智力障礙。我們發現 MCPH1可能通過調控BRCA1和CHK1...
Three: Growth/Development 17. Failure to Thrive 18. Obesity 19. Short Stature 20. Tall Stature 21. Weight Loss Section Four: Head 22. Abnormal Head Shape 23. Enlarged Anterior Fontanel 24. Facial Paralysis 25. Headache 26. Increased Intracranial Pressure 27. Macrocephaly 28. Microcephaly Section...
《小頭畸形相關蛋白WDR62在大腦皮層神經遷移中的功能研究》是依託福州大學，由徐丹擔任項目負責人的青年科學基金項目。項目摘要 常染色體隱性遺傳小頭畸形（autosomal recessive primary microcephaly, MCPH）是一種神經系統發育障礙疾病，病人主要表現為頭圍減小，並伴隨一定程度的智力障礙。核磁共振掃描結果顯示病人的...
Topics: Foundations of Pediatrics; HIV; Type 2 Diabetes; Angioedema and Anaphylaxis; Meningococcemia; Novel Pulmonary Endpoints in Clinical Trials; Inflammatory Mediators in Human Milk; Probiotics and Clinical Disease; Nutrition for Preterm Infants; Genetics of Microcephaly; Access to Healthcare Issues;...
13. Li C, Gao F, Yu L, Wang R, Jiang Y, Shi X, Yin C, Tang X, Zhang F, Xu Z, Zhang L. 2018. A Single Injection of Human Neutralizing Antibody Protects against Zika Virus Infection and Microcephaly in Developing Mouse Embryos. Cell Rep 23:1424-1434.14. Yu L, Wang R, Gao F...
2.Wei Zhang*, Si-Lu Yang*, Mei Yang, Stephanie Herrlinger, Qiang Shao, John Collar, Edgar Fierro, Yanhong Shi, Aimin Liu, Hui Lu, Bruce Herring, Zhen Zhao, and Jian-Fu Chen. Modeling microcephaly with cerebral organoids and mice reveals a WDR62-CEP170-KIF2A pathway promoting cilium ...
Li XH*, Guo D, Chen LQ, Chang ZH, Shi JX, Hu Nan, Chen C, Zhang XW, Bao SQ, Chen MM, Ming D*. Low-intensity ultrasound ameliorates brain organoid integration and rescues microcephaly deficits. Brain. 2024 May 13, Online ahead of print.Li XH*, Hu N, Chang ZH, Shi JX, Fan X,...
55. Ying Peng, Pai-hao Yang, Oscar G. Wong, Samuel S.M. Ng, Jie Liu, Ming-Liang He, Hsiang-fu Kung and Marie Lin*. A Critical Role of Pax6 in Alcohol-induced Fetal Microcephaly. Neurobiology of Disease 2004; 16 (2): 370-376.(IF:5.12)56. Ying Peng. Bing-Hua Jiang, Pai-...
XuS*, Sun X, Niu X, Zhang Z, Tian R, Ren W, Zhou K, Yang G* (2017)Genetic basis of brain size evolution in cetaceans: insights from adaptive evolution of seven primary microcephaly (MCPH) genes.BMC Evolutionary Biology,17:206 Tian R, Yin D, Liu Y, SeimI,Xu S*, Yang G* (...
