Kanemura T, Orii T, Ohtani M
Clin Genet. 1979 Dec;16(6):399-404. doi: 10.1111/j.1399-0004.1979.tb01348.x.
A 12-year-old by with unusual face and hearing loss was diagnosed as having frontometaphyseal dysplasia. He also had congenital urinary tract malformations and chronic urinary tract infection. The cranial and facial bones of the patient were studied by roentgen cephalometric analysis.
一名12岁面部异常且听力丧失的男孩被诊断为额骨干骺端发育异常。他还患有先天性尿路畸形和慢性尿路感染。通过X线头影测量分析对该患者的颅骨和面部骨骼进行了研究。
