Coco R, del Rey G
J Genet Hum. 1978 Dec;26(4):303-10.
A girl with multiple congenital malformations was found to have an abnormal karyotype: 46,XX,t(5;13) (13pter leads to 13q13 : : 5p14 leads to 5qter), meaning that she is monosomic for the distal part of the short arm of chromosome No. 5 (from 5pter to 5p14) and trisomic for the long arm of chromosome No. 13 (from 13q13 to 13qter). The proband's father is a carrier of a balanced reciprocal translocation: 46, XY, t(5;13) (p14;q13) (13qter leads to 13q13 : : 5p14 leads to 5qter; 13pter leads to 13q13 : : 5p14 leads to 5pter). Therefore, the propositus' abnormal karyotype was interpreted as the result from an adjacent type 1 malsegregation of the meiotic paternal quadrivalent MI22,IV (5p 14;13q13). Her phenotype agrees with the preliminar map of Noël et al. (1976) but, in addition, she shows craniosynostosis and practically normal psychomotor maturation.
46,XX,t(5;13) (13pter 至 13q13 : : 5p14 至 5qter),这意味着她5号染色体短臂远端部分(从5pter到5p14)单体型,13号染色体长臂(从13q13到13qter)三体型。先证者的父亲是平衡易位携带者:46, XY, t(5;13) (p14;q13) (13qter 至 13q13 : : 5p14 至 5qter; 13pter 至 13q13 : : 5p14 至 5pter)。因此,先证者的异常核型被解释为减数分裂时父本四价体MI22,IV(5p 14;13q13) 1型错误分离的结果。她的表型与诺埃尔等人(1976年)的初步图谱相符,但除此之外,她还表现出颅缝早闭,且精神运动发育基本正常。