Kääriäinen H, Ryöppy S, Norio R
Department of Medical Genetics, University of Helsinki, Finland.
Am J Med Genet. 1989 Jul;33(3):346-51. doi: 10.1002/ajmg.1320330312.
A new malformation syndrome is described in a pair of sibs and 3 sporadic patients. The characteristic manifestations are radial aplasia or hypoplasia, absence of thumbs, absent or hypoplastic patellae, dislocations of joints, unusual face, cleft or highly arched palate, diarrhea in infancy, small stature, and normal intelligence. Recessive inheritance seems the most plausible cause. The acronym RAPADILINO syndrome is proposed.
在一对同胞兄妹和3名散发病例中描述了一种新的畸形综合征。其特征性表现为桡骨发育不全或发育不良、拇指缺如、髌骨缺如或发育不全、关节脱位、面容异常、腭裂或高拱腭、婴儿期腹泻、身材矮小以及智力正常。隐性遗传似乎是最可能的病因。建议使用首字母缩略词RAPADILINO综合征。