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VACTERL综合征

VACTERL-association.

作者信息

Czeizel A, Ludányi I

出版信息

Acta Morphol Hung. 1984;32(2):75-96.

PMID:6435405
Abstract

The so-called 89 VACTERL cases i.e. three or more combinations of vertebral abnormalities (V), anal atresia (A), cardial abnormalities (C), tracheo-oesophageal fistula and/or oesophageal atresia (TE), renal agenesis and dysplasia (R), limb defect (mainly radial-type reduction or polydactyly) (L) were evaluated in the material of the Hungarian Congenital Malformation Register, 1970-1980. The separation of true VACTERL cases (without other major congenital abnormalities) and mixed VACTERL cases (with other major congenital abnormalities) seemed to be necessary. The latter may be a manifestation of several recognized syndromes. The VACTERL-association, i.e. three or more closely defined VACTERL-type abnormalities without other major abnormalities may, however, present a distinct congenital abnormality entity because (i) the combination of VACTERL-type abnormalities is much higher than the expected one, (ii) the majority of cases could not be identified as other multiple congenital abnormality entities and (iii) it has some epidemiological characteristics (e.g. male preponderance).

摘要

在匈牙利先天性畸形登记处1970 - 1980年的资料中,对所谓的89例VACTERL病例进行了评估,即椎体异常(V)、肛门闭锁(A)、心脏异常(C)、气管食管瘘和/或食管闭锁(TE)、肾发育不全和发育异常(R)、肢体缺陷(主要是桡骨型发育不全或多指畸形)(L)三种或更多种异常的组合。区分真正的VACTERL病例(无其他主要先天性异常)和混合性VACTERL病例(有其他主要先天性异常)似乎很有必要。后者可能是几种已确认综合征的表现。然而,VACTERL关联,即三种或更多种严格定义的VACTERL型异常且无其他主要异常,可能代表一种独特的先天性异常实体,原因如下:(i)VACTERL型异常的组合比预期的要高得多;(ii)大多数病例无法被认定为其他多种先天性异常实体;(iii)它具有一些流行病学特征(如男性占优势)。

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