Gedda L, Carrega R, Borgese L, Strollo F
Gregor Mendel Institute, Rome.
Acta Genet Med Gemellol (Roma). 1995;44(1):1-7. doi: 10.1017/s0001566000001835.
A healthy 23-year-old woman with amenorrhea was examined at the Mendel Institute. She had been amenorrheic for 4 years, and had not responded to hormone treatment. We therefore decided to study her family tree and karyotype. We describe the results of our study here: the patient was found to have gonadal dysgenesis, caused by translocation of a fragment of the X to a 12 chromosome, resulting from a break at q21, at the end of the q-arm.
一名23岁闭经的健康女性在孟德尔研究所接受了检查。她已经闭经4年,且对激素治疗无反应。因此,我们决定研究她的家族谱系和核型。我们在此描述研究结果:发现该患者患有性腺发育不全,是由于X染色体的一个片段易位到12号染色体,这是由q臂末端q21处的断裂所致。