Asano T, Ikeuchi T, Shinohara T, Enokido H, Hashimoto K
Department of Pediatrics, Nippon Medical School, Tokyo, Japan.
Jinrui Idengaku Zasshi. 1991 Sep;36(3):257-65. doi: 10.1007/BF01910544.
A 7-year-old boy with dysmorphic features was found to have a recombinant chromosome 18, rec(18), resulting from meiotic recombination of a maternal pericentric inversion, inv(18) (p11.2q21.3), as defined by high-resolution banding. He was trisomic for the long arm (q21.3-qter) and monosomic for the short arm (p11.2-pter) of chromosome 18. His clinical features were compared with those in other rec(18) cases, and also those in monosomy 18p, trisomy 18qter and full trisomy 18 syndromes. The risk of recombinant formation for inv(18) carriers was also discussed.
一名具有畸形特征的7岁男孩被发现有一条重组18号染色体,rec(18),这是由母亲的一条臂间倒位inv(18)(p11.2q21.3)减数分裂重组导致的,通过高分辨率显带确定。他18号染色体长臂(q21.3-qter)三体,短臂(p11.2-pter)单体。将他的临床特征与其他rec(18)病例以及18p单体、18qter三体和18号染色体完全三体综合征的病例进行了比较。还讨论了inv(18)携带者形成重组体的风险。