dysplasia
dysplasia
1. Australian Shepherd - retinal dysplasia occurs with other eye disorders, such as an oval pupil, microcornea (small cornea), cataracts, and retinal detachment.
#[[澳大利亚牧羊犬]]-与其他眼科疾病共发,例如椭圆瞳孔,小角膜,白内障和视网膜脱离.
2. The Bernese osteotomy has the advantages that are beyond other osteotomies. So it is the best to choose Bernese osteotomy for the treatment of teenaged or adult acetabular dysplasia.
Bernese术具有其它截骨术不可比拟的优势 ,是目前治疗青少年及成年髋臼发育不良的最佳选择。
3. Increased expression of proto oncogene c fos plays an important role in the occurence and development of fibrous dysplasia.
c?fos 癌基因的过度表达在骨纤维结构不良的发生发展中起重要作用。
4. CIN and cervical dysplasia may occur among childbearing aged women.
CIN及宫颈癌可发生于任何糜烂程度甚至光滑的宫颈;
5. HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
HHT是常染色体显性遗传性血管发育异常的一种疾病。
6. HP infection and the precancerous condition dysplasia are common in younger women.
HP感染和不典型增生的癌前期病变在年轻人里也很常见。
7. Dysplasia of cerebellum, and cystic enlargement of the fourth ventricle of cerebrum, and Dandy Walker syndrome were observed on MRI scanning.
MRI提示小脑发育不良,第4脑室囊状扩大,显示DandyWalker征象。
8. While the OFA continues to focus on hip dysplasia, the OFA has expanded into health screening for other inherited diseases and other companion animals such as cats.
OFA关注髋关节发育不良的同时，也对其他遗传疾病和伴侣动物如猫等，进行更广泛的健康审查。
9. The frequency of P 53 expression,the areas of positive expression of P 53 and the frequency of P 53 mRNA experession in JPS with dysplasia were significantly higher than those in JPS without dysplasia.
P53 蛋白阳性表达率、P53 阳性面积及P53 mRNA阳性表达率在JPS不典型增生组均显著高于JPS无不典型增生组。
10. PCNA, P53 protein, and Survivin may be valuable markers in assessing biological behavior of gastric epithelial dysplasia with intestinal metaplasia.
PCNA、P53和Survivin蛋白可作为判断胃异型增生上皮并肠上皮化生生物学行为有价值的指标。
11. IntroductionX-linked spondyloepiphyseal dysplasia tarda(SEDL, OMIM 313400) is a rare, X-linked recessive osteochondrodysplasia with an estimated prevalence of ~ 1.7 per million in Britain.
X-连锁迟发性脊椎骨骺发育不良(X-linked spondyloepiphyseal dysplasia tarda,SEDL,OMIM 313400)是一种罕见的遗传性骨软骨发育不良性疾病。
12. WANG Ying, WU Hua, ZHANG Xiao-xia, et al.Gene mutation detection in a cleidocranial dysplasia family[J].Chin J Stomatol, 2005, 40（6）：459-462.
[4] 王莹, 吴华, 张晓霞, 等. 家族性锁骨颅骨发育不全的基因突变 检测[J]. 中华口腔医学杂志, 2005, 40（6）：459-462.
13. Hip dysplasia is most common among larger breeds of dogs, especially German shepherds, rotweillers, Labrador retrievers, golden retrievers, mastiffs, and Saint Bernards.
‘髋关节发育不全’通常是一些大体型的品种容易得。
14. Hip dysplasia is most common among larger breeds, especially the German shepherd, rottweiler, Labrador retriever, golden retriever, mastiff, Saint Bernard, and others.
‘髋关节发育不全’通常是一些大体型的品种容易得。特别是“德国牧羊犬、罗威那犬、拉不拉多巡回犬、金毛巡回犬、马士提夫犬和圣伯那犬。
15. When the entire epithelium is dysplastic and no normal epithelial cells are left, then the process is beyond dysplasia and is now neoplasia.
一些部位象子宫颈上皮很容易发生恶变，肿瘤筛选常常选宫颈上皮细胞进行实验室检查。
16. Moderate Moderate Canine Hip Dysplasia: there is significant subluxation present where the ball is barely seated into a shallow socket causing joint incongruency.
中度髋关节发育不全：由于关节窝过浅,股骨头几乎没有固定进去关节窝中而形成一个显著脱出,造成髋关节的不契合。
17. She then underwent 99mTc-MDP bone scintigraphy the next day to evaluate the extent of polyostotic fibrous dysplasia.
为了瞭解多骨性纤维发育不良症病灶的范围，病人于隔日接受鎝-99m-MDP骨骼闪烁造影检查。
18. To evaluate clinical effect of transcranial optic nerve decompression on fronto orbito sphenoidal fibrous dysplasia with progressive vision loss, 25 cases were studied retrospectively.
为探讨因额眶蝶骨纤维结构不良致视力进行性下降经颅做视神经减压术的临床效果,作者对收治的25例次患者进行了回顾性研究。
19. Familialbilateral cystic dysplasia of kidneys.
为肾发育异常的弥漫性囊肿型。
20. Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia.
什么是'海伊井综合征-罕见的先天性条件影响皮肤头发和指甲'?
21. Cleidocranial dysostosis or Cleidocranial dysplasia is a hereditary congenital abnormality of humans due to haploinsufficiency caused by mutations in the CBFA1 gene.
什么是'锁骨颅骨发育不全-罕见的遗传性疾病导致矮身材'?
22. Dentin dysplasia is a genetic disorder of teeth, commonly exhibiting an autosomal dominant inheritance.
什麽是'牙本质发育异常-牙本质发育异常'?
23. For example, at a site in the Moravian region of the Czech Republic, three Paleolithic youngsters, one of whom was afflicted with congenital dysplasia, were discovered lying in unusual formation.
例如，在捷克共和国的摩拉维亚，三名旧石器时代的少年，其中一人饱受先天性发育不良之苦，被发现以奇怪的姿势躺着。
24. Learn what health problems are associated with this breed: hip dysplasia, digestive maladies, eye disorders, sebaceous adenitis (a genetic skin disease) and thyroid problems.
保持您狗狗的体重。过胖的狗狗容易有很多健康的问题，比如心脏病和关节炎。
25. In patients who had the functional disorder of hip joint resulting from hip diseases during their teen-ages, skeletal dysplasia and osteoporosis would occur.
儿童及青少年时期患髋关节疾患并造成髋功能障碍，易导致患侧肢体骨发育不良及骨质疏松。
26. Congenital absence of thenar muscles was seen in 14 hands of 8 patients, an d congenital dysplasia of fingers was seen in 4 hands of 3 patients.
其中,涉及拇指影响拇指功能的8例14侧,涉及其他手指或腕关节的3例4侧。统计受累肌肉以大鱼际肌为主,肌腱移位为主要的治疗方法。
27. These reealed one additional patient with dysplasia that was not detected by either technique.
利用每一检测技术检出病检中确诊为肿瘤形成的患者例数评估其诊断敏感性。
28. Developmental dislocation of the hip(DDH) is the most common disease in pediatric orthopedics, acetabular dysplasia, nonconcentric hip-joint articulation and approximate femoral deformity are the main pathologic morphology abnormality.
发育性髋关节脱位是小儿骨科最常见的先天性畸形之一，髋臼发育不良、股骨头脱位和股骨近端改变是髋关节脱位的主要骨性病理变化。
29. In other patients,pathological features showed 17 fibroedenoma,4 intraduct papilloma,2 breast cyst,10 mammary dysplasia and 1 caldfication without particular reason.
另外乳腺纤维瘤17例，导管内乳头状瘤4例，乳腺囊肿2例，乳腺腺病10例，不明原因钙化灶1例。
30. In 83.3%of the cases examined, exfoliated cells showing cytological dysplasia were found to be telomerase activity positive.
同时还测得83.3%的肺脱落细胞不典型增生者的端粒酶活性水平也显著增高。
31. Primary outcomes at 12 months included the complete eradication of dysplasia and intestinal metaplasia.
在12个月的时候，主要的结果包括发育异常和肠化生的彻底根治。
32. In 1974 data was published based on research on Great Dane puppies that concluded that there was a higher incidence of hip dysplasia in puppies fed a high protein, high energy, high mineral diet.
在1974年，依据大丹犬幼犬的数字被公布出来，当幼犬被喂食那些高蛋白质，高能量，高矿物元素的食品时，它们更容易发生髋关节结构变形的病症。
33. In the group treated with corton oil and CMV, dysplasia was found in 26.4% and cervical carcinoma in 52.8%.
在HCMV加巴豆油组，宫颈不典型增生的发生率为26.4%（14/53）。
34. In PL,with the progression of epithelial dysplasia,positive rate and positive stain intensity decreased gradually.
在PL组中，重度异常增生的阳性率最低。阳性染色强度随着异常增生程度的增加而减弱。
35. In Dalian, we are the first hospital developing acetabular rotary ostectomy to treat with adult acetabular dysplasia.
在创伤骨科方面，在各种复杂骨折的治疗上积累了丰富的经验，包括髋臼骨折、涉及关节的粉碎性骨折等。
36. Ectodermal dysplasia(ED)is an X-linked inherited disease.
外胚层发育不全为一遗传疾病，最常见的是性联缺汗性类型。
37. A multicystic dysplastic kidney (also known as cystic renal dysplasia) has been sectioned to reveal the variably sized cysts that replace the renal parenchyma.
多囊性发育不良肾也称为多囊肾发育不良，切开发现，大小不等的囊肿取代了肾实质。
38. Women : Amenorrhea, not ovulation, menstrual disorders, uterine fibroids and ovarian cysts and tubal nowhere, habitual abortion, uterine and ovarian endometriosis dysplasia, such as polycystic syndrome.
女性：闭经、不排卵、月经不调、子宫肌瘤、卵巢囊肿、输卵管不通、习惯性流产、卵巢及子宫发育不良子宫内膜异位症、多囊综合症等。
39. Women: Amenorrhea, not ovulation, menstrual disorders, uterine fibroids and ovarian cysts and tubal nowhere, habitual abortion, uterine and ovarian endometriosis dysplasia, such as polycystic syndrome.
女性：闭经、排卵、经不调、宫肌瘤、巢囊肿、卵管不通、惯性流产、巢及子宫发育不良子宫内膜异位症、囊综合症等。
40. And if left untreated, dysplasia will become cerical cancer.
如果不治疗不典型增生将发展为子宫颈癌。
41. Endocervix:moderate dysplasia of the cervix with loss of polarity of slightly hyperchromatic nuclei over the lower half of the squamous epithelium.
子宫颈内膜:中等程度分化不良，鳞状上皮下半部细胞核已失去排列极性。
42. Severe dysplasia in children with familial adenomatous polyposis:Rare or simply overlooked?
家族性腺瘤样息肉病患儿的重度不典型增生:是否罕见或仅是被忽略
43. Familial Calvarial Doughnut Lesions-A Variant of Fibrous Dysplasia?
家族性颅骨圈饼状病灶-纤维性分化不良变异型？
44. The interest in intestinal metaplasia stems from studies that hae consistently demonstrated intestinal metaplasia and dysplasia both adjacent to and remote from esophageal adenocarcinoma.
对肠化生的兴趣来源于一些研究,他们一贯认为肠化生和不典型增生或多或少与食管腺癌有关.
45. Hypohydrotic ectodermal dysplasia is a common group of hereditary diseases, with congenital tooth loss as the predominant oral symptom.
少汗型外胚层发育不良症是一类相对常见的遗传性综合性疾病,先天性牙缺失是此类疾病的主要口腔表现。
46. Batty had x-rays a couple of weeks ago and hip dysplasia was not evident.
弹琴伴奏的男人是一个很出色的音乐家。
47. Cyclic follicular dysplasia is also known as seasonal alopecia.
循环性毛囊发育不良又称季节性脱毛.
48. In XLSA, the function of stem cells is primarily normal before erythropoiesis, then the erythroid progenitors become dysplasia.
患者的干细胞功能大致正常，定向分化到红系造血后才出现异常。
49. Chronic gastritis with intestinal metaplasia, negative for dysplasia or malignancy.
慢性胃炎伴肠化，无异型增生或恶性肿瘤。
50. The operation to correct hip dysplasia produced an abnormality in acetabular anteversion.
手术可改变髋臼前倾角，部分会至异常范围。
51. This paper reported a rarely seen case with hypohidrotic ectodermal dysplasia.
报告1例少汗性外胚叶发育不全病例。
52. This article reports a case of anhidrotic ectodermal dysplasia associated with giant type granuloma annulare.
报告1例无汗性外胚叶发育不良伴巨大型环状肉芽肿。
53. Casseus suffers from a rare form of polyostotic fibrous dysplasia, a nonhereditary, genetic disease that causes bone to become swollen and jelly-like.
据美联社12月17日报道，美国迈阿密杰克逊纪念医疗中心的医生们表示，12月14日进行的那次长达16个多小时的手术很成功。
54. There was dysplasia in the peri carcinoma.Conclusin: EEC could occur multicentrically.
提示临床医生在胃镜检查应注意多点取材,以防漏诊;
55. Abstract : Abstract Objective To study the incidence,risk factors,prophylaxis and treatment for bronchopulmonary dysplasia (BPD) in premature.
摘要 ： 目的 分析早产儿支气管肺发育不良(BPD)的发生率和危险因素，探讨防治BPD的措施。
56. A seven-year-old boy with a retrovesical dive rticulum and ipsilateral renal dysplasia is reported.
摘要一位七岁男童患有先天性膀胱憩室，这是一种少见的异常。
57. To determine the accuracy of hip arthrography in developmental dysplasia of the hip (DDH), we studied 11 patients with DDH who had undergone 12 hip arthrographies between 1990 and 1993.
摘要为了探讨髋关节摄影对于髋关节发育障碍的诊断价值，我们回溯性研究1990年至1993年间，本院11例髋关节发育障碍的病患，共有12组髋关节摄影，以其结果和手术的发现作一比较。
58. Conventional ventilators have their limitations in management of certain conditions such as protracted hypercarbia in bronchopulmonary dysplasia (BPD).
摘要传统的呼吸器在某些情况，例如肺支气管发育不良患者的高二气化碳血症的治疗上，是有其极限；
59. Ectodermal dysplasia(ED)is an X-linked inherited disease.The most common is the hypohidrotic X-linked form affecting male subjects.
摘要外胚层发育不全为一遗传疾病，最常见的是性联缺汗性类型。
60. Ectodermal dysplasia appears in two froms, hidrotic and anhidrotic, according to clinical features and hereditary characteristics.
摘要外胚层异常症，依照临床表徵及遗传特性，可分成无汗型与出汗型两大类。
61. Arrhythmogenic right ventricular dysplasia is a rare disease that sometimes leads to sudden death in young people.
摘要心律不整性右心室发育不全是一种少见的疾病，但是也是造成轻人猝死的主要原因之一。
62. Congenital anhidrotic ectodermal dysplasia is a rare inherited disease.Here, we report a 56 years old male with the chief complaint of blurred vision &had never sweat since childhood.
摘要本文报告-无汗性外胚层发育不良之病例，患者为56岁男性，主诉视力减退。
63. Objective: To study the expression of CDK2 in hamster buckle pouch normal mucosa、hyperplasia、dysplasia and squamous cell carcinoma.
摘要目的：探讨CDK2在金黄地鼠颊囊黏膜从正常黏膜到单纯增生、异常增生及鳞癌的表达变化。
64. Objective: To investigate the clinical and genetic features of ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome (EEC) in Chinese kindreds.
摘要目的：探讨先天缺指（趾）-外胚叶发育不良-唇／腭裂综合征(EEC)的临床表型和遗传学特点。
65. Objective: To define the ultrasonographic feature of mammary dysplasia so as to improve diagnostic accuracy of the condition.
摘要目的：探讨女性乳腺结构不良声像图的特征，提高对该病的诊断水平。
66. Objective: To investigate the X-ray and CT manifestations of familial cleidocranial dysplasia.
摘要目的：探讨家族性锁骨颅骨发育不全的X线及CT表现特征。
67. Objective: To estimate the recent operative effect of total hip arthroplasty and constructural bone graft for the hip dysplasia accompanied by necrosis of femur head.
摘要目的：评价全髋关节置换、结构性植骨治疗髋臼发育不良伴股骨头坏死的近期手术效果。
68. Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.
摘要致死性畸胎是最常见的致死性新生儿侏儒症其特点为短小的四肢、小胸、巨头及脑部发育异常等。
69. Myelodysplastic syndromes are refered to as a group of diseases characterized by abnormal clonal proliferation of hematopoietic stem cells with pancytopenia and dysplasia.
摘要骨髓增生异常综合徵是以造血干细胞的异常克隆性增生、血细胞减少、骨髓出现病态造血为特徵的一类疾病。
70. Methods Thirty seven cases were treated with cross reticular bone grass used in SAA, including developmental dysplasia of the hip (DDH) and coax plana caused by Legg-Perthes disease.
方法 对发育性髋关节发育不良、大龄髋关节半脱位、Legg Perthes病扁平髋的患者 37例采用交叉网状植骨方式槽状髋臼扩大术治疗。
71. Methods The expression of Ki 67, CD34 and apoptosis were evaluated by SP immunohistochemical staining in 15 BLOM, 9 BLOM with dysplasia, 15 oral squamous cell carcinoma (OSCC).
方法 采用免疫组化SP法检测 15例黏膜良性淋巴组织增生病、9例黏膜良性淋巴组织增生病伴上皮异常增生、15例口腔癌及 10例正常黏膜组织中Ki 6 7的表达、细胞凋亡及微血管密度。
72. Methods: We retrospectively studied the CT imaging of 47 cases which had been proved to be fibrous dysplasia by surgery pathology.
方法:回顾性分析47例经手术病理证实的骨纤维异常增殖症患者的CT表现并与之对比。
73. Methods: All 38 cases of maxillary fibrous dysplasia underwent surgical excision to spade up the hyperplastic tissues for shape or excised the pathological maxilla.
方法:对38例上颌骨骨纤维异常增殖症患者均采用手术治疗铲除增生的组织,修整形态或彻底切除病变组织。
74. Methods: Peripheral blood samples were obtained from three different families of hypohidrotic ectodermal dysplasia.
方法:对3个少汗性外胚叶发育不全核心家系进行外周血基因组DNA的提取。
75. Method 12 cases with congenital acetabular dysplasia were treated with rotational acetabular osteotomy.All patients were clinically reviewed after operation.
方法:对我院应用髋臼旋转截骨术治疗的12例髋臼发育不良患者的疗效进行回顾性分析。
76. Methods:Patients with cleidocranial dysplasia were examined,recorded,made photos and analyzed with x-ray films.
方法:对颅骨锁骨发育不全综合征患者进行体检,建立病历,摄片,分析牙、颌面及影像特点。
77. Methods The treatment of 10 cases of cranialfacial fibrous dysplasia was analyzed.
方法分析10例颅面部骨纤维结构不良患者的不同手术方法。
78. Methods:The X-ray and CT findings and clinical sym ptoms in 6 cases (2 families) with cleidocranial dysplasia were analysed, and d iscussed on genetic basis.
方法分析6例(2个家庭)锁骨颅骨发育不全的临床、X线及CT表现,并从遗传学角度进行探讨。
79. Methods:Retrospective review of three cases of thanatophoric dysplasia.
方法复习1438例尸检中诊断为致死性侏儒的3例作回顾性研究。
80. Methods The CT and MRI findings in 16 pediatric and adult cases with corpus callosum dysplasia were reviewed.
方法对16例儿童和成人胼胝体发育不全患者的CT和MRI表现进行分析,并讨论其诊断作用。
