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另外網站One lung ventilation in a patient with Seckel Syndrome也說明:CONCLUSION. Understanding of the constellation of features present in Seckel syndrome and their impact on airway management is crucial for practitioners.
中臺科技大學 護理系碩士班 林冠語所指導 覺筱韻的 到院前心跳停止病患行目標體溫管理對 臨床預後之影響-以中部某區域教學醫院為例 (2021),提出Seckel syndrome關鍵因素是什麼,來自於到院前心跳停止、目標體溫管理、臨床預後因子、併發症。
而第二篇論文國立政治大學 中東與中亞研究碩士學位學程 林季平所指導 鍾雨珊的 從法國2012年至2020年本土聖戰主義攻擊:探討移民後代參與本土恐怖攻擊之因素 (2020),提出因為有 社會排斥、世代斷裂、暴力學習、社會認同、團體動力的重點而找出了 Seckel syndrome的解答。
最後網站Seckel syndrome exhibits cellular features demonstrating ...則補充:Abstract. To date, the only reported genetic defect identified in the developmental disorder, Seckel syndrome, is a mutation in ataxia telangiectasia and ...
到院前心跳停止病患行目標體溫管理對 臨床預後之影響-以中部某區域教學醫院為例
為了解決Seckel syndrome 的問題,作者覺筱韻 這樣論述:
「到院前心跳停止」(Out-of-Hospital Cardiac Arrest),是搶時間的急症,即使恢復心跳後,仍可能因心跳停止後症候群(Post Cardiac Arrest Syndrome),造成神經系統損害。國際準則建議在360分鐘內介入目標體溫管理(Target temperature management),可有效增加存活率和改善神經學。本研究以中部某區域醫院2014- 2020間,以TTM介入OHCA治療者,分為黃金達溫組65名及延遲達溫組62名,共計127名。透過電子病歷回顧進行資料收集分析。以SPSS 19.0 for Windows 統計軟體進行描述性和推論性分析。基
本屬性顯示,OHCA好發於男性(61%)、高齡(44%)、體重過重、疾病嚴重度高(p < .05)及過去病史複雜。併發疾病中,肺炎、泌尿道感染、敗血性休克、腸胃道出血(p < .000;p < .000;p < .006;p < .028),在黃金達溫組發生率低於延遲達溫組。也證實在360分鐘內到達目標體溫,可獲得較佳的神經功能預後及減少死亡率。 OHCA病患只有一次重生機會,因此應盡快開始低溫治療,使TTM小於360分鐘,以減少住院期間感染發生及提高神經系統結果和存活率,有利於提升OHCA患者存活率及長期照護品質。
從法國2012年至2020年本土聖戰主義攻擊:探討移民後代參與本土恐怖攻擊之因素
為了解決Seckel syndrome 的問題,作者鍾雨珊 這樣論述:
法國2015年11月13日巴黎恐怖攻擊後,移民後代的整合問題再度成為安全議題的核心,綜觀歐洲,參與本土聖戰的移民後代中約有一半來自法國,為理解移民後代是否因「社會排斥」產生挫折,進而攻擊自己成長的國家,以釐清「社會整合」是否為有效的反恐手段,因此本文以移民後代參與本土聖戰人數、比例最高的法國作為個案分析。本文第二章從結構層次,假設「社會排斥」為移民後代的挫折來源,根據聯合國的指標分為:宗教文化、政治外交、經濟機會及社會接納四大面向,探討「社會排斥」是否為移民後代參與本土聖戰的充分條件,但由於本土聖戰攻擊者在整體法國移民後代中比例極低,因此第三章前兩節,本文從個人層次討論移民後代與原生家庭和社
區的「世代斷裂」及負面詮釋的「人格特質」,是否削弱他們對於「社會排斥」的抗壓性,進而提高參與攻擊的可能性。其次,有些移民後代在主觀上雖沒有明顯挫折經驗,但「社會排斥」帶來的「向下流動」使他們生活於犯罪猖獗的郊區,因此對暴力使用司空見慣;此外,網路媒體的發達也讓未接觸過暴力的移民後代,得以開啟聖戰的大門,因而第三章的後兩節探討「暴力學習經驗」是否為移民後代的充分條件。最後,筆者觀察到因為殖民遺緒,外國聖戰組織中擁有大量來自法語國家的重要幹部,這些聖戰士返國後建立據點,利用「社會認同」或「團體動力」吸引法國移民後代參與聖戰,這些聖戰新兵又透過親密關係影響自己的親友及伴侶,使聖戰網絡得以擴張,而在這
個過程中,有些本土聖戰攻擊者不一定有「挫折」或「暴力學習」經驗,因此本文在第四章主張「團體因素」是法國移民後代加入本土聖戰的充分條件,而「挫折」或「暴力學習」經驗則是在團體的基礎上,發揮催化的作用。
想知道Seckel syndrome更多一定要看下面主題
Seckel syndrome的網路口碑排行榜
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#1.Seckel Syndrome with Polyarteritis Nodosa - Indian Pediatrics
Seckel syndrome is a rare genetic disorder with a typical “bird-headed” appearance. It could affect many organ systems but renal involvement is. 於 www.indianpediatrics.net -
#2.Test | Invitae Microcephalic Primordial Dwarfism and Seckel ...
The Invitae Microcephalic Primordial Dwarfism and Seckel Syndrome Panel analyzes genes that are associated with disorders causing microcephalic primordial ... 於 www.invitae.com -
#3.One lung ventilation in a patient with Seckel Syndrome
CONCLUSION. Understanding of the constellation of features present in Seckel syndrome and their impact on airway management is crucial for practitioners. 於 scholarlycommons.libraryinfo.bhs.org -
#4.Seckel syndrome exhibits cellular features demonstrating ...
Abstract. To date, the only reported genetic defect identified in the developmental disorder, Seckel syndrome, is a mutation in ataxia telangiectasia and ... 於 academic.oup.com -
#5.Seckel syndrome 9 - UniProt
Definition. A form of Seckel syndrome, a rare autosomal recessive disorder characterized by proportionate dwarfism of prenatal onset associated with low birth ... 於 www.uniprot.org -
#6.Ocular manifestations of Seckel syndrome - American Journal ...
Seckel syndrome is a rare autosomal recessive disorder characterized by severe psychophysical deficiency and unique physiognomy. 於 www.ajo.com -
#7.Seckel Syndrome With Asymptomatic Tonsillar Herniation and ...
Seckel syndrome is a rare genetic disorder of recessive inheritance characterized by prenatal-onset growth retardation, abnormally small head, ... 於 journals.sagepub.com -
#8.Seckel Syndrome - Contemporary OB/GYN
Seckel syndrome is a form of primordial dwarfism with a set of primary diagnostic criteria, however, there are also several secondary ... 於 www.contemporaryobgyn.net -
#9.Verification and rectification of cell type-specific splicing of a ...
Seckel syndrome (SS, OMIM: 210600) is a spectrum of congenital disorders that mainly exhibit intrauterine growth defects resulting in severe ... 於 www.nature.com -
#10.somal fragility in a patient with features of Seckel syndrome
We report a patient with Seckel syndrome with myelodysplastic features and clonal T-cells in the bone marrow but no evidence of chromosomal fragility. After 5 ... 於 www.haematologica.org -
#11.Seckel syndrome: A report of a case Ramalingam K ...
Seckel syndrome is a rare constellation of malformations, presumably inherited as an autosomal recessive inherited trait. The male to female sex ... 於 www.jisppd.com -
#12.Seckel syndrome - APA Dictionary of Psychology
Seckel syndrome a familial disorder, now linked to a defect on chromosome 3 (locus 3q22.1–24), marked by microcephaly, a beaklike nose, prominent eyes, ... 於 dictionary.apa.org -
#13.Seckel syndrome: A case report of the rare syndrome - Gale
Seckel syndrome is a rare genetic disorder characterized by marked intra-uterine growth retardation (primordial dwarfism) and post natal dwarfism, ... 於 go.gale.com -
#14.Seckel Syndrome and Primordial Dwarfism - Verywell Health
Seckel syndrome is an inherited form of primordial dwarfism, meaning that an infant starts out very small and fails to grow normally after ... 於 www.verywellhealth.com -
#15.Seckel syndrome: report of a case - Allen Press
Parent P, Moulin S, Munck MR, de Parscau L, Alix D. Bird headed dwarfism in Seckel syndrome. Nosologic difficulties. Arch Pediatr 3: 55–62, 1996 ... 於 meridian.allenpress.com -
#16.The Primordial Dwarfisms: Diagnosis, Identification of the ...
Condition or disease. Microcephalic Osteodysplastic Primordial Dwarfism Type II Seckel Syndrome. Detailed Description:. 於 clinicaltrials.gov -
#17.seckel syndrome and epilepsy - Thieme Connect
Objectives: Seckel syndrome is a very rare autosomal recessive disorder characterized by growth retardation, severe microcephaly with a bird-headed like ... 於 www.thieme-connect.com -
#18.Seckel syndrome | Radiology Reference Article - Radiopaedia
Seckel syndrome is an autosomal recessive congenital dwarfing disorder. Epidemiology The estimated incidence is ~1:10000. 於 radiopaedia.org -
#19.SECKEL SYNDROME : CASE REPORTS - Journal of The ...
Seckel syndrome is an autosomal recessive disorder characterized by intrauterine growth retardation and post-natally by dwarfism, severe microcephaly, ... 於 journal.kapd.org -
#20.Perinatal Findings of Seckel Syndrome: A Case Report of a ...
Objective/Methods: Seckel syndrome is a rare form of primordial dwarfism and most of the previous reports have been limited to postnatal ... 於 www.karger.com -
#21.Bilateral retinal detachment in Seckel syndrome - Canadian ...
Seckel syndrome, a rare inherited disorder characterized by severe psychophysical deficiency and unique physiognomy, was first described by ... 於 www.canadianjournalofophthalmology.ca -
#22.Seckel syndrome: an overdiagnosed syndrome - Journal of ...
Seckel syndrome is only one of a group of low birth weight microcephalic dwarfism and careful attention should be paid to fulfilment of the ... 於 jmg.bmj.com -
#23.Seckel Syndrome - NORD (National Organization for Rare ...
Seckel syndrome is rare genetic condition with slow growth before birth (intrauterine growth restriction) resulting in low birth weight. 於 rarediseases.org -
#24.Prenatal diagnosis of Seckel syndrome at 21 weeks' gestation ...
Background: The Seckel syndrome is an autosomal recessive inherited disorder that characterized severe pre- and post-natal growth restriction, ... 於 www.tandfonline.com -
#25.STUDY CASE - Redalyc
REPERCUSSIONS OF SPEECH THERAPY IN SECKEL SYNDROME: STUDY CASE. Revista CEFAC, vol. 17, núm. 5, septiembre-octubre, 2015, pp. 1698-1715. Instituto Cefac. 於 www.redalyc.org -
#26.An anesthetic experience in a patient with Seckel syndrome
Seckel syndrome is an autosomal recessive, primordial dwarfism. The clinical symptoms and signs include severe intrauterine and postnatal growth retardation ... 於 ekja.org -
#27.Seckel syndrome (NGS panel of 11 genes) - CGC Genetics
Seckel syndrome (NGS panel of 11 genes). ATR, CENPJ, CEP152, CEP63, DNA2, LIG4, NIN, ... Genetic syndromes with skeletal involvement (NGS panel of 38 genes) ... 於 www.cgcgenetics.com -
#28.Seckel syndrome and centrosomal protein Ninein localizes ...
Ninein (Nin) is a centrosomal protein whose gene is mutated in Seckel syndrome (SCKL, MIM 210600), an inherited recessive disease that results in primordial ... 於 diginole.lib.fsu.edu -
#29.Seckel syndrome Disease Ontology Browser - DOID:0050569
Mutations in human and/or mouse homologs are associated with this disease. ... Harper's syndrome; microcephalic primordial dwarfism; Virchow-Seckel dwarfism. 於 www.informatics.jax.org -
#30.Seckel syndrome. A case report - Medigraphic
Seckel syndrome, is a genetic disorder characterized by microcephaly, prominent nose, very short stature, caused by mutations in the gene whose locus have ... 於 www.medigraphic.com -
#31.A Case of Cerebral Dystrophy and Cerebellar Atropy in Seckel ...
Seckel syndrome is a rare autosomal recessive disease. The characteristic features of Seckel syndrome include Intrauterine and postnatal growth deficiency, ... 於 www.annchildneurol.org -
#32.Seckel Syndrome and Pregnancy: The Importance of ... - JOGNN
Seckel syndrome is an extremely rare autosomal recessive genetic disorder that is a form of primordial dwarfism and was first described in 1960 by Dr. Sekel ... 於 www.jognn.org -
#33.Seckel Syndrome Accompanied by Semilobar ...
Seckel syndrome is a rare autosomal recessive disorder, and its characteristic features include prenatal and postnatal growth retardation, microcephaly, ... 於 www.pedneur.com -
#34.Cranial MRI findings in a case with Seckel syndrome - DergiPark
Seckel's syndrome (SS) is a rare, heterogeneous form of primordial dwarfism. The presence of mental retardation and neurologic signs is one of the peculiar ... 於 dergipark.org.tr -
#35.Seckel Syndrome - Walking With Giants Foundation
If any parent or guardian visiting this site thinks their child has a form of Microcephalic Primordial Dwarfism, they should consult a local Clinical Geneticist ... 於 www.walkingwithgiants.org -
#36.POMS: DI 23022.296 - Seckel Syndrome - 08/28/2020 - Social ...
Seckel syndrome (SCKL) is a rare genetic disorder characterized by growth delays prior to birth (intrauterine growth retardation), ... 於 secure.ssa.gov -
#37.Seckel syndrome Help Entry H00992 Disease Name - KEGG ...
Seckel syndrome is a recessively inherited dwarfism characterized by intrauterine growth retardation, proportionate postnatal dwarfism, severe microcephaly, ... 於 www.kegg.jp -
#38.ZFIN Human Disease: Seckel syndrome
Synonyms: bird-headed dwarfism; Harper's syndrome; microcephalic primordial dwarfism; Virchow-Seckel dwarfism. (all 4). Definition: A syndrome characterized ... 於 zfin.org -
#39.Seckel Syndrome - Causes, Symptoms, Diagnosis, Treatment ...
Seckel syndrome is a rare genetic condition that is inherited in an autosomal recessive manner. This means that the chance of both the copies of ... 於 www.medindia.net -
#40.Seckel Syndrome with Spontaneous Chromosomal Instability
Abstract: Seckel syndrome is an autosomal recessive disorder characterized by prenatal and postnatal growth retardation, bird-headed face and mild mental ... 於 citeseerx.ist.psu.edu -
#41.The Seckel Syndrome: A Case Observed in the Pediatric ...
Seckel syndrome -1 or “bird-headed dwarfism”, Online Mendelian Inheritance in Man number 210600, is a rare genetic disease with an autosomal recessive ... 於 www.mdpi.com -
#42.Seckel syndrome - wikidoc
One form of Seckel syndrome can be caused by mutation in the gene encoding ataxia-telangiectasia and RAD3-related protein ATR which maps to ... 於 www.wikidoc.org -
#43.New Comprehensive Testing for Seckel syndrome!
Seckel syndrome belongs to the microcephalic osteodysplastic dwarfism group characterized by intrauterine growth retardation, dwarfism, ... 於 dnatesting.uchicago.edu -
#44.Two Cases of Seckel Syndrome.
Seckel syndrome is a rare, autosomal recessive disorder of severe growth retardation and distinct craniofacial, orodental, and skeletal anomalies. 於 e-apem.org -
#46.OMIM Entry - # 210600 - SECKEL SYNDROME 1; SCKL1
Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with mental retardation, ... 於 www.omim.org -
#47.Management of seckel syndrome: a pediatric case report
4 Characteristic features of this syndrome include severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and ... 於 medcraveonline.com -
#48.Seckel syndrome - Warsaw Genomics
than 1 in 1 million newborns. There are distinctive forms of Seckel syndrome based on their genetic cause. Genes and genetic syndromes. Gen. Choroba/objawy. 於 warsawgenomics.pl -
#49.Seckel Syndrome 5/ Microcephaly 9 (CEP152) - Sema4
Seckel syndrome (SCKL5) and Microcephaly 9 (MCPH9) are allelic disorders caused by pathogenic variants in the gene CEP152. Onset of SCKL5 is in utero and ... 於 sema4.com -
#50.SECKEL SYNDROME - Little People of Ontario
Seckel syndrome is one of six diagnoses in the family of "primordial dwarfism". The condition is divided into different types, which involve genetic ... 於 littlepeopleofontario.com -
#51.A case report of the rare syndrome Mahesh N, Sathish S ...
Seckel syndrome is a rare genetic disorder characterized by marked intra-uterine growth retardation (primordial dwarfism) and post natal ... 於 www.jdrntruhs.org -
#52.Seckel syndrome - Global Genes
Overview. Type of disease: Rare conditions. Seckel syndrome is a genetic disorder characterized by growth retardation, microcephaly with mental retardation, ... 於 globalgenes.org -
#53.Seckel Syndrome NGS Panel | Genetic Testing Lab - DDC ...
This panel includes the most common genes associated with Seckel syndrome, an autosomal recessive disorder. 於 www.ddccliniclab.org -
#54.Seckel Syndrome - Kaiser Permanente
Seckel syndrome is an extremely rare inherited disorder characterized by growth delays prior to birth (intrauterine growth retardation) ... 於 wa.kaiserpermanente.org -
#55.Nephrolithiasis in a 17-Year-Old Male With Seckel Syndrome ...
We report the case of a 17-year-old male with Seckel syndrome and horseshoe kidneys which had a 7 mm kidney stone in the lower pole calyx of ... 於 www.goldjournal.net -
#56.Seckel Syndrome and Social Security Disability
Seckel Syndrome is a congenital disorder that causes a particular type of dwarfism. The disorder is marked by stunted growth in and out of the womb, ... 於 www.disability-benefits-help.org -
#57.Seckel syndrome | Encyclopedia.com
Seckel syndromeDefinitionSeckel syndrome is an extremely rare inherited disorder characterized by low birth weight, dwarfism, a very small head, ... 於 www.encyclopedia.com -
#58.Seckel syndrome Definition & Meaning | Dictionary.com
An inherited disorder characterized by low birth weight, dwarfism, microcephaly, large eyes, beaked nose, receding chin, and mental retardation.Seckel ... 於 www.dictionary.com -
#59.Bird-headed dwarfs (Seckel's syndrome) - The Journal of ...
Bird-headed dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies. 於 www.jpeds.com -
#60.Primordial Dwarfism: A Case Series From North East of Iran ...
Seckel Syndrome (SS) is a rare autosomal recessive disorder (4) and first defined by Seckel in 1960. He described 2 case studies by himself and 13 cases ... 於 jpediatricsreview.com -
#61.Cataract in Seckel Syndrome | Semantic Scholar
A patient with Seckel syndrome who had bilateral cataracts and underwent uneventful small incision cataract surgery in both eyes is described. 於 www.semanticscholar.org -
#62.Seckel Syndrome: Disease Bioinformatics - Novus Biologicals
Learn more about Seckel Syndrome from related diseases, pathways, genes and PTMs with the Novus Bioinformatics Tool. 於 www.novusbio.com -
#63.Repercussions of speech therapy in Seckel syndrome - SciELO
Seckel syndrome, it's rare condition of autosomal recessive hereditary nature of, characterized by severe growth retardation, intrauterine, ... 於 www.scielo.br -
#64.Seckel Syndrome News, Research
Seckel Syndrome News and Research · Researchers identify potential new treatment for brain cancer by targeting genes linked to microcephaly · Study identifies ... 於 www.news-medical.net -
#65.Primary microcephaly case from the Karachay-Cherkess ...
Population screening reveals allele frequency to be less than 0.005. Mutations in this gene were not previously associated with Seckel syndrome. 於 bmcmedgenomics.biomedcentral.com -
#66.Seckel syndrome with cutaneous pigmentary changes: two ...
Seckel syndrome (SCKL) is an extremely rare form of primordial dwarfism characterized by growth delay, proportionate extreme short stature, ... 於 www.termedia.pl -
#67.Seckel syndrome and moyamoya in - Journal of Neurosurgery
Seckel syndrome is an autosomal recessive disorder characterized by intrauterine and postnatal growth delay, microcephaly with mental retardation, ... 於 thejns.org -
#68.A Child with Seckel Syndrome and Arterial Stenosis: Case ...
Background: Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is characterized by dysmorphic features, ... 於 www.dovepress.com -
#69.Concise Encyclopedia of Special Education: A Reference for ...
Children with Seckel syndrome have moderate to severe mental retardation ( Jones , 1988 ) . These children often exhibit hyperactive behavior and have ... 於 books.google.com.tw -
#70.Seckel Syndrome - an overview | ScienceDirect Topics
Seckel (SCKL) syndrome, sometimes called “bird-headed dwarfism,” is an autosomal recessive developmental disorder characterized by marked growth failure and ... 於 www.sciencedirect.com -
#71.Seckel syndrome - Wikipedia
Seckel syndrome, or microcephalic primordial dwarfism is an extremely rare congenital nanosomic disorder. Inheritance is autosomal recessive. 於 en.wikipedia.org -
#72.The Seckel syndrome and centrosomal protein Ninein ...
Ninein (Nin) is a centrosomal protein whose gene is mutated in Seckel syndrome (SCKL, MIM 210600), an inherited recessive disease that ... 於 www.molbiolcell.org -
#73.Seckel syndrome, causes, symptoms, diagnosis, treatment ...
Seckel syndrome is characterized by abnormally slow growth during fetal development (intrauterine growth retardation [IUGR] with average birth weight 1540g), ... 於 healthjade.net -
#74.Seckel syndrome with Morgagni hernia - Lippincott
Seckel syndrome is an autosomal recessive disease presenting with microcephalic dwarfism, mental retardation and facial and skeletal abnormalities. 於 journals.lww.com -
#75.Medical Definition of Seckel syndrome - RxList
Seckel syndrome : A birth defect syndrome with severe short stature and, characteristically, low birth weight, very small head (microcephaly), ... 於 www.rxlist.com -
#76.Seckel Syndrome - Oxford Medicine Online
Seckel syndrome belongs to the family of Microcephalic Primordial Dwarfisms (MPDs), a clinically heterogeneous group of conditions associated with growth ... 於 oxfordmedicine.com -
#77.Seckel Syndrome - AccessAnesthesiology
"Seckel Syndrome." Syndromes: Rapid Recognition and Perioperative Implications Bissonnette B, Luginbuehl I, Marciniak B, Dalens BJ. Bissonnette B, & Luginbuehl ... 於 accessanesthesiology.mhmedical.com -
#78.Genetic testing for Seckel syndrome
Seckel Syndrome Panel · Is a 6 gene panel that includes assessment of non-coding variants. · Is ideal for patients with a clinical suspicion of Seckel Syndrome. 於 blueprintgenetics.com -
#79.Seckel syndrome - Orphanet
A rare form of microcephalic primordial dwarfism characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly, a typical dysmorphic face ( ... 於 www.orpha.net -
#80.Lia, Mama Diva, Penyandang Seckel Syndrome - JawaPos.com
Lia, Mama Diva, Penyandang Seckel Syndrome: Remuk Redam Anak Dicaci. SEMATA WAYANG: Lia Octoratrisna bersama putrinya, Diva, 17. 於 www.jawapos.com -
#81.SECKEL SYNDROME IN A - 2 YEAR OLD GIRL | Medicina
Abstract. Seckel syndrome is a frequent autosomal recessive that cause microcephalic osteodysplastic dwarfisms. It characterized with proportionate dwarfism ... 於 ojs.unud.ac.id -
#82.Skeletal and Neurological Features of Seckel Syndrome and ...
2020年9月14日 — Method: Medical Databases search was done for the Keywords: Seckel Syndrome, MOPD and Microcephalic Osteoplastic Primordial Dwarfism. All ... 於 www.researchgate.net -
#83.A case observed in the pediatric department of the University ...
Seckel syndrome -1 or “bird-headed dwarfism”, Online Mendelian Inheritance in Man number 210600, is a rare genetic disease with an autosomal ... 於 www.pagepress.org -
#84.A new locus for Seckel syndrome on chromosome 18p11.31 ...
Seckel syndrome (MIM 210600) is a rare autosomal recessive disorder with a heterogeneous appearance. Key features are growth retardation, microcephaly with ... 於 pure.au.dk -
#85.Seckel Syndrome - Medical Resource Center
Seckel syndrome. Source/Author: Geneva Foundation for Medical Education and Research Web-based (medical) Photographs and fetal ultrasound images of ... 於 lpamrs.memberclicks.net -
#86.Mengenal Disabilitas Langka Seckel Syndrome dan Terapinya
Seckel Syndrome adalah disabilitas bawaan yang terjadi akibat kelainan genetik. Disabilitas ini termasuk ke dalam jenis disabilitas fisik ... 於 www.liputan6.com -
#87.Test | Seckel Syndrome, Primary Microcephaly and Familial ...
Seckel Syndrome, Primary Microcephaly and Familial Cutaneous Telangiectasia and Cancer Syndrome via the ATR Gene. Order Options and Pricing. 於 www.preventiongenetics.com -
#88.Seckel syndrome - Genetic and Rare Diseases Information ...
Medical Terms Other Names Learn More:HPO ID Cachexia Wasting syndrome 0004326 Clinodactyly of the 5th finger Permanent curving of the pinkie finger 0004209 Craniosynostosis ‑ ‑‑> 0001363 於 rarediseases.info.nih.gov -
#89.Seckel Syndrome 2 (SCKL2) - MalaCards
Seckel Syndrome 2 (SCKL2). Categories: Bone diseases, Eye diseases, Fetal diseases, Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases, Smell/ ... 於 www.malacards.org -
#90.Seckel Syndrome(塞克尔综合征) - 皮肤病学 - 天山医学院
皮肤病治疗大全➢与皮肤病有关的综合征〕塞克尔综合征(Seckel Syndrome)又称鸟头样侏儒Montreal型(bird-headed dwarfism,Montreal type)、魏尔啸-塞克尔综合 ... 於 www.tsu.tw -
#91.Cardiovascular anomalies in Seckel syndrome: report of two ...
Seckel syndrome is a very rare autosomal recessive disorder also known as bird headed dwarfism”. It is characterised by proportional short ... 於 www.cambridge.org -
#92.Seckel syndrome - 塞克爾氏症 - 國家教育研究院雙語詞彙
Seckel syndrome. 以Seckel syndrome 進行詞彙精確檢索結果. 出處/學術領域, 英文詞彙 ... 於 terms.naer.edu.tw -
#93.CtIP Mutations Cause Seckel and Jawad Syndromes - PLOS
Seckel syndrome is a recessively inherited dwarfism disorder characterized by microcephaly and a unique head profile. 於 journals.plos.org -
#94.Rita G. Harper • LITFL • Medical Eponym Library
Rita Gilman Harper (1934 - ) American pediatrician. Harper syndrome (1967) synonym for Seckel syndrome or microcephalic primordial dwarfism. 於 litfl.com -
#95.KEGG DISEASE: Seckel syndrome
Seckel syndrome is a recessively inherited dwarfism characterized by intrauterine growth retardation, proportionate postnatal dwarfism, severe microcephaly, ... 於 www.genome.jp -
#96.New drug candidate for Seckel syndrome|News and Events
Seckel syndrome is a rare genetic disease that causes slow growth in the womb. Dwarfism and microcephaly are common effects, the latter ... 於 www.cira.kyoto-u.ac.jp