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唇(牙槽突及腭)裂或腭裂患者伴发的面部发育异常。

Concomitant developmental anomalies of the face in patients with clefts of lip (alveolus, and palate) or cleft palates.

作者信息

Gundlach K K

出版信息

Scand J Plast Reconstr Surg Hand Surg. 1987;21(1):27-30. doi: 10.3109/02844318709083575.

DOI:10.3109/02844318709083575
PMID:3589575
Abstract

Out of 2,829 cleft patients of Nordwestdeutsche Kieferklinik Hamburg 356 were found to have additional pathologic findings in the head and neck area. It was noted that the greater the dimension of the cleft, the greater the number of concomitant anomalies. However, the severity of the additional malformation could not be correlated to the severity of clefting. All additional pathologic findings were classified according to Pfeifer's morphogenetic classification of craniofacial anomalies. In cleft patients the region most often affected was found to be the lateral (and posterior) parts of the head. However, in unilateral clefts it was not possible to correlate the location of the cleft to the location of the concomitant malformation.

摘要

在汉堡西北德国颌面外科诊所的2829例腭裂患者中,发现356例在头颈部区域有其他病理发现。值得注意的是,腭裂范围越大,伴随畸形的数量就越多。然而,额外畸形的严重程度与腭裂的严重程度并无关联。所有额外的病理发现均根据法伊费尔的颅面异常形态发生分类法进行分类。在腭裂患者中,发现最常受影响的区域是头部的外侧(和后侧)部分。然而,在单侧腭裂中,无法将腭裂的位置与伴随畸形的位置联系起来。

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