亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Classification for congenital anomalies of the hand: the IFSSH classification and the JSSH modification.

畸形 医学 手部畸形 解剖 外科
作者
De Smet L
出处
期刊:PubMed [National Institutes of Health]
卷期号:13 (3): 331-8 被引量:13
链接
标识
摘要

The purpose of a classification for clinical problems which, except for a few specialized centers, occur only sporadically is to provide a system where these cases can be stored. This should allow all involved investigators to speak the same language; so-doing syndromes can be delinated, frequencies of occurence established and results of--different--treatments compared. A classification system should be simple to use, reliable and uniformly accepted. It should allow space for adaptations and/or extensions. The IFSSH proposed a 7 categories classification based on the proposed classification of Swanson et al. in 1976. This classification, was based on, which was thought in the seventies, etiopathogenic pathways. These 7 groups are: I. Failure of formation; transverse (A), or longitudinal (B) II. Failure of differentiation III. Polydactyly IV. Overgrowth V. Undergrowth VI. Amniotic band syndrome VII. Generalized skeletal syndromes. The extended classification proposed by IFSSH was used to classify 1013 hand differences in 925 hands of 650 patients. We found associated anomalies in 26.7%. The classification was straightforward in 86%, difficult in 6.6% and not possible in 7.8%. Group II was the most numerous group including 513 anomalies. We propose to include in this group the Madelung deformity, the Kirner deformity and congenital trigger fingers and trigger thumbs. In group I the radial and ulnar deficiencies, limited to the hand without forearm deficlencies should be Included. Triphalangeal thumbs are a problem, we suggest it to be listed in group III and consider it as a duplication in length. It is not always possible to evaluate the (transverse) absence of the fingers or hand. Longitudinal deficiencies (group IIB), symbrachydactyly (group V), and amniotic bands (group IV) occasionally develop a phenotype similar to the genuine transverse deficiency (group IA). Recently, the Japanese Society for Surgery of the Hand (JSSH) (16) proposed an extension/modification of the IFSSH classification. Based on newer knowledge on teratology, symbrachydactyly in all stages were transfered to group I. Two new groups were introduced. A group "failure of finger ray induction" including typical cleft hand (IC), central polydactyly (III) and (bony) syndactyly (II)--was included. Also a group of "unclassifiable" cases was added. This Japanese proposed classification is a real improvement and most clinicians and surgeons tend to use it in the future.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
soilman发布了新的文献求助30
刚刚
2秒前
多情的涔完成签到,获得积分10
5秒前
佳豪师弟发布了新的文献求助10
7秒前
ARESCI完成签到,获得积分20
15秒前
佳豪师弟完成签到,获得积分10
15秒前
Orange应助ARESCI采纳,获得10
18秒前
Kaylaa完成签到,获得积分10
21秒前
CJH104完成签到 ,获得积分10
25秒前
Re完成签到 ,获得积分10
30秒前
科研通AI6.2应助soilman采纳,获得10
36秒前
41秒前
soilman发布了新的文献求助10
47秒前
fabius0351完成签到,获得积分10
59秒前
神璃完成签到,获得积分10
1分钟前
清秀灵薇完成签到,获得积分10
1分钟前
1分钟前
1分钟前
甜甜诗筠完成签到,获得积分10
1分钟前
甜甜诗筠发布了新的文献求助10
1分钟前
豆豆完成签到,获得积分10
1分钟前
贺安完成签到 ,获得积分10
1分钟前
研友_VZG7GZ应助科研通管家采纳,获得10
1分钟前
1分钟前
1分钟前
Kaylaa关注了科研通微信公众号
2分钟前
2分钟前
吴函城完成签到,获得积分10
3分钟前
rcheng完成签到,获得积分10
3分钟前
3分钟前
3分钟前
3分钟前
3分钟前
许海沨发布了新的文献求助50
4分钟前
霸气的灵竹应助许海沨采纳,获得10
4分钟前
Kevin完成签到 ,获得积分10
4分钟前
科研通AI6.4应助soilman采纳,获得10
4分钟前
4分钟前
楚楚完成签到 ,获得积分10
4分钟前
嗯对完成签到 ,获得积分10
4分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Nondestructive Testing Handbook: Vol. 4, Thermal and Infrared Testing (IR), 4th ed 800
作者名:Kristopher P. Plain,悉尼大学的,目前只能查到其四篇论文,想找到其博士论文 590
Évora na Idade Média 555
Soil mites of the family Rhagidiidae (Actinedida: Eupodoidea). Morphology, Systematics, Ecology 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Radical Reactions 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7362933
求助须知:如何正确求助?哪些是违规求助? 8972098
关于积分的说明 19071435
捐赠科研通 7008445
什么是DOI,文献DOI怎么找? 3223677
关于科研通互助平台的介绍 2387360
邀请新用户注册赠送积分活动 2204424