Asthana J C, Sinha S, Haslam J S, Kingston H M
Community Child Health, Tameside and Glossop Health Authority.
Arch Dis Child. 1990 Oct;65(10):1133-6. doi: 10.1136/adc.65.10.1133.
A diagnostic survey was undertaken of children aged 11 to 19 years in Tameside with severe learning difficulties (intelligence quotient less than or equal to 50). Eighty-two children were identified and their medical records reviewed. A specific diagnosis for the retardation was documented in 25 (30%) of the children, 18 of whom had Down's syndrome. A probable aetiology or a disorder of unknown aetiology had been identified in a further 21 (26%) children. To confirm the existing diagnosis, identify new diagnoses, and offer genetic counselling, the parents of 63 children were offered detailed reassessment of their child. Fifty three children were reviewed, and a specific disorder identified in 25 out of 31 previously undiagnosed children. The most frequent diagnoses made were fragile X syndrome and Rett's syndrome. On completion of the survey, 61 of the 82 children (74%) had a specific diagnosis or probable aetiology identified, 12 (15%) had associated disorders such as cerebral palsy, and in only nine of the 82 children (11%) were there no clues at all to the cause of their retardation.
对泰姆赛德地区11至19岁有严重学习困难(智商小于或等于50)的儿童进行了一项诊断性调查。共识别出82名儿童,并对他们的病历进行了审查。25名(30%)儿童的发育迟缓有明确诊断记录,其中18名患有唐氏综合征。另有21名(26%)儿童确定了可能的病因或病因不明的病症。为了确认现有诊断、发现新诊断并提供遗传咨询,为63名儿童的家长提供了对其子女的详细重新评估。对53名儿童进行了复查,在31名先前未确诊的儿童中有25名确定了具体病症。最常见的诊断是脆性X综合征和瑞特综合征。调查结束时,82名儿童中有61名(74%)确定了具体诊断或可能的病因,12名(15%)有诸如脑瘫等相关病症,82名儿童中只有9名(11%)完全没有发育迟缓原因的线索。