Bianchi D W
Am J Med Genet. 1984 Oct;19(2):383-6. doi: 10.1002/ajmg.1320190221.
A 30-week premature male infant is presented with dolichocephaly, frontal bossing, down-slanting palpebral fissures, hypertelorism, long philtrum, micrognathia, cleft palate, and imperforate anus. He is the fifth patient to be presented with FG syndrome and sensorineural deafness. The patient's syndromic manifestations became more obvious during an inpatient observation period of 3 months.
一名30周早产男婴，表现为长头畸形、额部隆突、睑裂向下倾斜、眼距增宽、人中长、小颌畸形、腭裂和肛门闭锁。他是第五例患有FG综合征和感音神经性耳聋的患者。在3个月的住院观察期内，该患者的综合征表现变得更加明显。
