Bhattacharyya Ranjan, Sanyal Debasish, Bhattacharyya Sumita
Department of Psychiatry, Murshidabad Medical College and Hospital, Berhampore, West Bengal, India.
Department of Psychiatry, KPC Medical College and Hospital, Jadavpur, Kolkata, West Bengal, India.
Indian J Psychiatry. 2018 Oct-Dec;60(4):398-403. doi: 10.4103/psychiatry.IndianJPsychiatry_401_17.
Down syndrome, most common chromosomal abnormality leading to intellectual disability is being diagnosed by Karyotyping. Due to cost constraints, parents couldn't afford to do Karyotyping which causes delay in individual and family interventions.
Down syndrome has characteristic morphological features. The minor physical anomaly (MPA) are insults which occur in utero during embryonic development mostly in first and early second trimester and persists throughout life.
70 karyotyping confirmed cases of Down syndrome (DS), 70 other causes of intellectual disabilities (Other ID) and 70 age matched normal children and adolescents (Average) have been incorporated in the study. The Modified Waldrop's scale (Ismail's 41 item scale) have been applied. Demographic comparison and Decision tree algorithm approach have been analysed by SPSS 25 version.
The paternal age of childbirth, maternal age of childbirth, maternal age of marriage ( < 0.001), income ( = 0.026) variables are statistically significant in Down's syndrome group in comparison to other two groups whereas age and birth order are not statistically significant. DS group has more MPA (m = 17.04, SD = 5.462), than other ID (m = 5.93, SD = 2.628) and Average group (m = 1.59, SD = 1.378). Big sandal gap, high arched palate and epicanthus are most common three minor anomalies found in Down syndrome. Region wise scoring shows high significance ( < 0.001) in Global head, eyes, ears, mouth, hands and feet in Down syndrome group. The four anomalies; epicanthus, telecanthus, high-arched palate, and curved fifth finger) thus can be grouped as differentiating anomalies. When clinodactyly (item 27) and high arched palate (item 21) are present together or epicanthus (item 08) and telecanthus (item 09) present together sensitivity of diagnosing the case as Down syndrome is 0.945 with negative predictive value 0.979.
The simian crease which is being considered as common physical anomaly is not specific for Down syndrome. The large scale study is required to extrapolate the above findings but surely it opens new avenue of research.
唐氏综合征是导致智力残疾最常见的染色体异常疾病,目前通过核型分析进行诊断。由于成本限制,家长负担不起核型分析的费用,这导致个体和家庭干预的延迟。
唐氏综合征具有特征性的形态学特征。轻微身体异常(MPA)是指在胚胎发育期间,主要是在孕早期和孕中期早期发生在子宫内的损伤,并持续终生。
本研究纳入了70例经核型分析确诊的唐氏综合征(DS)病例、70例其他智力残疾原因(其他ID)的病例以及70例年龄匹配的正常儿童和青少年(平均组)。应用了改良的沃尔德罗普量表(伊斯梅尔的41项量表)。通过SPSS 25版本对人口统计学比较和决策树算法方法进行了分析。
与其他两组相比,唐氏综合征组的孩子父亲生育年龄、母亲生育年龄、母亲结婚年龄(<0.001)、收入(=0.026)变量具有统计学意义,而年龄和出生顺序则无统计学意义。唐氏综合征组的轻微身体异常(MPA)(m = 17.04,SD = 5.462)比其他智力残疾组(m = 5.93,SD = 2.628)和平均组(m = 1.59,SD = 1.378)更多。大草鞋间隙、高拱腭和内眦赘皮是唐氏综合征中最常见的三种轻微异常。按区域评分显示,唐氏综合征组在全球头部、眼睛、耳朵、嘴巴、手和脚方面具有高度显著性(<0.001)。因此,内眦赘皮、睑裂增宽、高拱腭和弯曲第五指这四种异常可归为鉴别性异常。当小指内弯(第27项)和高拱腭(第21项)同时出现,或内眦赘皮(第08项)和睑裂增宽(第09项)同时出现时,将病例诊断为唐氏综合征的敏感性为0.945,阴性预测值为0.979。
被认为是常见身体异常的猿线对唐氏综合征并不具有特异性。需要进行大规模研究来推断上述发现,但这无疑开辟了新的研究途径。