Reiser C A, Pauli R M, Hall J G
Am J Med Genet. 1984 Oct;19(2):245-50. doi: 10.1002/ajmg.1320190206.
We review six families in which recurrence of achondroplasia, inexplicable through autosomal dominant inheritance, has occurred. The clinical and radiographic characteristics of affected individuals in these families are identical to those usually seen in achondroplasia. Family histories and parental characteristics likewise seemed not to set this group apart from others with achondroplasia. While various mechanisms for these occurrences of achondroplasia in family members related through unaffected relatives can be postulated, the hypothesis that these recurrences were simply the result of two independent chance events cannot, at least for the moment, be excluded.
我们回顾了六个出现软骨发育不全复发的家族,这种复发无法通过常染色体显性遗传来解释。这些家族中受影响个体的临床和放射学特征与软骨发育不全通常所见的特征相同。家族病史和父母特征同样似乎并未使这一组人与其他软骨发育不全患者区分开来。虽然可以推测通过未受影响亲属相关的家庭成员中这些软骨发育不全病例出现的各种机制,但至少目前不能排除这些复发仅仅是两个独立偶然事件结果的假设。