Halal F, Picard J L, Raymond-Tremblay D, de Bosset P
Am J Med Genet. 1982 Sep;13(1):71-9. doi: 10.1002/ajmg.1320130112.
We report the familial occurrence in a French Canadian family of metaphyseal dysplasia associated to short stature and previously undescribed facial and acral anomalies. Facial manifestations include beaked nose, short philtrum, thin lips, maxillary hypoplasia, dystrophic yellowish teeth. Acral changes include bilateral shortness of metacarpal 5 and/or 2nd middle phalanx of fingers 2 and 5. Dermatoglyphics show low TRC, distal or absent axial triradius, absent triradius C, and radial loop on digit 4. The syndrome appears to be an autosomal dominant trait.
我们报告了一个法裔加拿大家庭中发生的干骺端发育异常,该异常与身材矮小以及此前未描述的面部和肢端异常相关。面部表现包括鹰嘴鼻、人中短、嘴唇薄、上颌骨发育不全、营养不良性黄牙。肢端改变包括双侧第5掌骨短和/或第2和第5指的第2中节指骨短。皮纹学显示总嵴纹数低、远侧轴三叉点缺失或不存在、C三叉点缺失以及第4指为桡侧箕形纹。该综合征似乎是一种常染色体显性性状。