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Results All the children and their parents received interviews, otological examinations and clinical audiolugical teats. Their ages were between 4 and 15, with the average at 9.51±2.83.①The males were 341 (61.66%) and female 212 (38.34%), with the gender ratio of male to female as 1.61:1.②The peak of the age curves of treatment and the first onset of vertigo was 9.51 and 8.62-year-old, respectively.③20.98% of children with vertigo had normal results with peripheral vertigo more common in the rest.④ The semicircular canals were more likely to dysfunction if their relatives had vertigo or car sickness.

结果 ①553例儿童年龄4~15岁，平均9.51±2.83岁；男341例(61.66%)、女212例(38.34%)，男女之比为1.61：1；②就诊年龄和初次眩晕发病年龄的高峰期分别在9.51岁和8.62岁，发病无季节性，主要症状为自身或视物旋转，发作持续时间为数分钟至数小时；③约20.98%的儿童眩晕患者各项检查结果均正常，异常组中以外周性眩晕多见(78.04%， 341/437)，半规管功能异常者占63.83%(353/553)；④256例眩晕儿童直系家属中有眩晕史，其中171例(66.80%)出现水平半规管功能异常。

The early treatment of cheiloschisis and palatoschisis include the treatment and nursing of postnatal physiological dysfunction, physiognomy defect, developmental malformation, secondary maxillofacial malformation and psychic health of the patient and the parents.

唇腭裂早期治疗是对唇腭裂患儿出生后存在的生理功能障碍、外貌缺陷、以及随生长发育畸形的变化、术后继发的牙颌系统畸形、患儿及父母的精神心理健康问题进行一系列治疗护理，直到成为身心康复的个体。

The reason of the disease is uncertain and its pathologic change is chronic Inflammation of joints, cell infiltration, information of pannus and the erosion of cartilage and bones, which lead to the destruction and dysfunction of joints structure.

本病病因未明，主要病理变化为关节滑膜的慢性炎症细胞浸润、血管翳形成、软骨及骨组织的侵蚀，导致关节结构的破坏和功能丧失。

The second phenotype, adrenomyeloneuropathy, manifests most commonly in the late twenties as progressive paraparesis, sphincter disturbances, sexual dysfunction, and often, impaired adrenocortical function; all symptoms are progressive over decades.

第二个表型是肾上腺髓质神经病，症状通常是在25岁至30岁间出现渐行性下肢轻瘫、括约肌障碍、性功能障碍和经常性的肾上腺皮质功能障碍；所有的症状都是在几十年间渐行的。

Spinal neurological involvement was defined by the neurological examination findings suggestive of spinal localization such as paraparesis, sensory deficits indicating a spinal level and sphincter and/or sexual dysfunction or a combination of them.

本研究收集了自1984年以来我院神经白塞病中心收治的所有白塞病脊髓受累患者；所有患者均符合国际白塞病研究小组确定的白塞病诊断标准；同时，通过检查有无脊髓定位体征如截瘫、感觉平面、括约肌和/或性功能障碍等，来确定患者是否有脊髓受累。

Sensory impairment and urinary dysfunction also had developed, and paraparesis persisted after the hypokalemia was corrected during hospitalization. An optokinetic nystagmus test showed bilateral sick waves and at the same time a cerebrospinal fluid analysis was normal. A blood examination disclosed borderline anti-nuclear antibodies and an elevated serum IgG level. Her cervical spinal cord showed mild swelling and contrast-enhancement when examined by magnetic resonance imaging. Neither a brain stem nor an optic nerve's lesion was found. Based on the above, acute transverse myelitis was diagnosed. All the symptoms present in the patient relieved gradually after 5-days of pulsed intravenous methylprednisolone therapy.

一50岁女性，因为眩晕、前额头痛、视力模糊、恶心、呕吐及两侧下肢无力而求诊，於低血钾矫正后，两侧下肢无力依然持续，并发生胸部以下感觉缺损及排尿困难等现象，视运动性眼振检查显示两侧波形障碍，脑脊液检查正常，血液学检查显示抗核酸抗体及血清IgG指数偏高，显影剂增强磁振造影显示颈段脊髓肿大且略为显影，并无脑干或视神经的病灶，诊断为急性横断性脊髓炎，给予静脉注射类固醇后症状逐渐缓解。

The results suggest that assessment of hip-muscle performance should be considered in the evaluation and treatment of patellofemoral joint dysfunction.

该结果提示评价和治疗髌股骨关节功能障碍，应考虑进行髋部肌肉行为评估。

Of serious malformation, in particular also with severe pectus excavatum cardiopulmonary dysfunction sick child should be given surgery.

对严重的畸形，特别是漏斗胸又合并严重心肺功能障碍的病儿，则应给予外科手术治疗。

A serious deformity, especially in pectus excavatum with severe cardiopulmonary dysfunction also the sick child should be given to surgery.

严重畸形，特别是在漏斗，严重心肺功能障碍的患病儿童也应考虑手术。

Pectus excavatum, and chicken breast with severe heart and lung dysfunction in rare cases, deformity is not serious child, with age, physical development can be corrected.

漏斗胸和鸡胸合并严重心肺功能障碍的病例并不多见，畸形不严重的幼儿，随年龄增长、身体的发育还可有所矫正。

So it was last week in Selma , alabama.

上星期在亚拉巴马州塞尔马市发生的事件也是这样一个转折点。

The group also spearheads various social programs in China.

该组织还带头参与中国的各种社会活动。