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一种基于八个体征的新生儿唐氏综合征诊断评分。

A score based on eight signs in the diagnosis of Down syndrome in the newborn.

作者信息

Fried K

出版信息

J Ment Defic Res. 1980 Sep;24(3):181-5. doi: 10.1111/j.1365-2788.1980.tb00072.x.

Abstract

Experience with a score based on eight signs of Down syndrome is described. The signs are: (1) abundant neck skin, (2) mouth corners turned downward, (3) general hypotonia (4) flat face, (5) dysplastic ear, (6) epicanthic eye-fold, (7) gap between first and second toes, (8) protruding tongue. Examination was done in the first week of life of the newborn to evaluate his score. About five minutes were spent to score a child. An infant with a score of 6, 7, or 8 (showing 6, 7, or 8 signs) is considered clinically proven Down syndrome. When an infant has a score of 0, 1, or 2, the diagnosis is disproved. No false positive or false negative were observed among approximately 19,000 liveobrn infants born in this hospital in a five-year period (1973--1977). All the thirty infants where the diagnosis was considered were karyotyped, twenty-six had regular trisomy 21, and four had a normal karyotype. Of the twenty-one initially suspected cases who were checked for the score, twenty had a score of 6--8 (all had a karyotype of trisomy 21), only one had a score of 0--2 (she had a normal karyotype), and eight had a score of 3--5. This last group is heterogenous as it included five affected infants and three children with a normal karyotype and is the only group where cytogenetic investigation is indicated for diagnostic purposes. It is suggested that this score should be used routinely for the clinical evaluation of every newborn where the possibility of a diagnosis of Down syndrome has been raised.

摘要

本文描述了一种基于唐氏综合征八个体征的评分方法。这些体征包括:(1)颈部皮肤丰富;(2)嘴角向下;(3)全身肌张力低下;(4)面部扁平;(5)耳部发育异常;(6)内眦赘皮;(7)第一和第二脚趾间有间隙;(8)舌头外伸。在新生儿出生后的第一周进行检查以评估其得分。给一个孩子评分大约需要五分钟。得分6、7或8(显示出6、7或8个体征)的婴儿被临床诊断为唐氏综合征。当婴儿得分为0、1或2时,可排除该诊断。在该医院五年期间(1973 - 1977年)出生的约19,000名活产婴儿中,未观察到假阳性或假阴性情况。所有被考虑进行诊断的30名婴儿都进行了染色体核型分析,其中26名有典型的21 - 三体,4名染色体核型正常。在最初怀疑的21例接受评分检查的病例中,20例得分为6 - 8(所有染色体核型均为21 - 三体),只有1例得分为0 - 2(其染色体核型正常),8例得分为3 - 5。最后一组情况较为复杂,其中包括5名患病婴儿和3名染色体核型正常的儿童,这是唯一一组需要进行细胞遗传学检查以明确诊断的情况。建议在每例疑似唐氏综合征的新生儿临床评估中常规使用该评分方法。

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