Svinhufvud E, Myllärniemi S, Norio R
Municipal Health Centre, Tuusula, Finland.
Clin Genet. 1988 Dec;34(6):373-81. doi: 10.1111/j.1399-0004.1988.tb02895.x.
Four kindreds with family-specific malposition of cuspids were studied. Besides malposition of cuspids, the members also showed varying combinations of other anomalies: malposition, malformation or hypodontia of upper lateral incisors, second bicuspids and lower central incisors. The pedigrees provided convincing evidence for autosomal dominant transmission of the abnormalities studied. Their nature and location allow the assumption that they represent different expressions of one dominant gene causing a primary disturbance in the critical marginal area of the embryonic dental lamina.
对四个患有特定家族性尖牙错位的家族进行了研究。除了尖牙错位外,这些家族成员还表现出其他异常的不同组合:上颌侧切牙、第二双尖牙和下颌中切牙的错位、畸形或牙缺失。这些系谱为所研究异常的常染色体显性遗传提供了令人信服的证据。它们的性质和位置使人认为,它们代表了一个显性基因的不同表现形式,该基因在胚胎牙板的关键边缘区域引起原发性紊乱。