发育迟缓

Results Of the 181 patients, there were 109 cases of the West syndrome (60%), 60 cases of non West syndrome epilepsy (33%), and 11 cases with no convulsive history (6%).

结果 181例表现高峰节律紊乱的患者中婴儿痉挛 10 9例(6 0 %)，非West综合征癫痫 6 0例(33%)，没有惊厥病史者 11例(6 %)，包括精神运动发育迟缓 7例(4 %)，Rett综合征 3例(2 %)。

However, correction of the problem is not through food restriction, which can secondarily lead to immune suppression, stunting, debilitation from multiple nutrient deficiencies, and shortened lifespan, but through increasing humidity.

所以问题的根本不是限制食物，这会造成免疫力下降，发育迟缓，疲劳等等一些营养缺乏症状，并且会影响龟龟的寿命。

Second, the impact of calcium and phosphorus metabolism, thereby affecting the normal function of bones, causing bone decalcification, bone atrophy, bone density decrease, the elderly and children, osteoporosis, rickets and dental growth retardation.

其次，影响钙和磷的代谢，进而影响骨骼的正常功能，造成骨脱钙、骨萎缩、骨密度降低、中老年人骨质疏松症和儿童佝偻病及牙齿生长发育迟缓。

Especially in the intrauterine growth retardation, and take a left decubitus treatment can achieve better results.

特别是在胎儿发育迟缓时，采取左侧卧位可使治疗取得更好效果。

Results After one-year theray, 70% of patients with delayed language achieved the expected target and most dysarthria were corrected.

结果 经过 1年的治疗，70 %的语言发育迟缓患儿达到预期的训练目标，大部分构音障碍患儿得到矫正。

Aphasia, dysarthria,delayed language development,hearing disorder,speech disorder of cerebral palsy, stutter can be evaluated ,diagnosed and intevented. The patients can get best hearing aid fitting and intervention here.

失语症，构音障碍，儿童语言发育迟缓，听力障碍、口吃、脑瘫儿童的语言障碍不仅可以得到及时准确的评价和诊断，还能得到最好的治疗。

Disease characteristics. Homocystinuria caused by cystathionine β-synthase deficiency is characterized by developmental delay/mental retardation, ectopia lentis and/or severe myopia, skeletal abnormalities (excessive height and length of the limbs) and thromboembolism.

疾病特征：由胱硫醚β-合酶缺乏引起的高胱氨酸尿症的病征是发育迟缓／智力障碍、晶状体异位和／或严重的近视骨骼异常和血栓栓塞。

Other features include birth weight, growth and growth retardation, mental retardation, small head, round face, low ears, eyes from too broad, muscle tight low-end, on epicanthus, palm, and so on.

其它特点还包括出生时体重轻、生长及发育迟缓、智能不足、小头、圆脸、低位耳、眼距过宽、肌肉紧结性低、上眦赘皮、断掌等。

Results All of the 8 cases were abnormal in ultrasonography. There were more than 2 parts of anomalies in 7 cases (7/8), heart anomalies in 5 cases (5/8), holoprosencephaly in 2 cases (2/8), single umbilical artery in 2 cases (2/8), Dandy-walker syndrome in 1 case (1/8), and other anomalies such as cleft lip and cleft palate, diaphragmatic hernia, omphalocele, esophageal atresia, malformation of radius, club hand, club foot. Four cases were polyhydrmnios and 3 cases were IUGR.

结果 8例18三体综合征胎儿声像图均表现为胎儿结构异常，7例(7/8)超声表现为两个部位以上畸形，5例(5/8)合并心脏畸形，2例(2/8)为全前脑，2例(2/8)为单脐动脉，1例(1/8)为Dandy-walker综合征，其他畸形还有唇腭裂、膈疝、脐膨出、食道闭锁、桡骨发育不良、手畸形、马蹄内翻足、小下颌。4例(4/8)合并羊水过多，3例(3/8)宫内发育迟缓。

Reik W. Genomic imprinting. Imprinting with and without methylation. Curr Biol, 1994, 4(2):145-147.[4] Yoshioka H, Shirayolshi Y, 0shimura M.

PWS的临床症状主要有肌张力低下、身材矮小、外生殖器发育不良和精神发育迟缓等。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。