Murphy G, Hulse J A, Jackson D, Tyrer P, Glossop J, Smith I, Grant D
Arch Dis Child. 1986 Aug;61(8):761-5. doi: 10.1136/adc.61.8.761.
Eighty children from the North West and North East Thames Regional Health Authorities who had been identified as having congenital hypothyroidism either by neonatal screening (76 cases) or by clinical symptoms (four) were seen for psychological assessments at 1 (60 cases), 3 (58), and/or 5 (20) years of age. Almost all the children's scores were in the normal range, and comparisons with matched controls suggested that they were doing only slightly less well than normal children in overall development. They were significantly slower, however, on a motor skills task. Moreover, a low initial serum thyroxine and triiodothyronine value, considerable delay in initial bone age, and an absence of thyroid tissue on isotope scan seemed to be associated with a somewhat poorer prognosis.
来自西北和东北泰晤士河地区卫生局的80名儿童,通过新生儿筛查(76例)或临床症状(4例)被确诊为先天性甲状腺功能减退症,他们在1岁(60例)、3岁(58例)和/或5岁(20例)时接受了心理评估。几乎所有儿童的得分都在正常范围内,与匹配的对照组相比,他们在整体发育方面仅略逊于正常儿童。然而,他们在一项运动技能任务上明显较慢。此外,初始血清甲状腺素和三碘甲状腺原氨酸值较低、初始骨龄明显延迟以及同位素扫描显示无甲状腺组织,似乎与预后稍差有关。