Zamboni G, Bernardi F, Danesino C, del Majno U M, Beghini G, Dalla Bernardina B
J Med Genet. 1980 Feb;17(1):59-61. doi: 10.1136/jmg.17.1.59.
A case of agenesis of the corpus callosum with a chromosomal abnormality is reported. The patient was a male infant, born to phenotypically normal, non-consanguineous parents. He had an abnormal phenotype, mental retardation, and chromosome mosaicism 46,XY/47,XY,+r. Chromosomal analysis of both parents showed a normal karotype. The origin of the small ring chromosome could not be determined and it is difficult to relate the phenotype of the infant to the cytogenetic findings.
报告了一例胼胝体发育不全伴染色体异常的病例。患者为男婴,其父母表型正常,非近亲结婚。他有异常表型、智力发育迟缓以及染色体嵌合体46,XY/47,XY,+r。对其父母进行的染色体分析显示核型正常。小环状染色体的起源无法确定,且难以将婴儿的表型与细胞遗传学结果联系起来。