Denaro A, Rossi M, Garozzo A, Saita V, Nicotra S, Catalano C, Angrì F
Istituto di Clinica Otorinolaringoiatrica, Università di Catania.
Minerva Pediatr. 1990 Jan-Feb;42(1-2):35-40.
The paper reports the case of a newborn affected by malformations of the middle parts of the face. The patient was described as cebophalus according to Kundrat's classification because he had a single nostril, hypotelorism and severe brain malformations. Prosencephalia is present in 0.5% of all aborted fetuses but is very rare in live births (0.006%). Survival is extremely short and in this case the patient lived for 12 months. A description of the malformations is given using CT scans.
该论文报告了一名面部中部畸形的新生儿病例。根据昆德拉特分类法,该患者被描述为无脑儿,因为他有一个鼻孔、眼距过窄和严重的脑部畸形。前脑无裂畸形在所有流产胎儿中占0.5%,但在活产中非常罕见(0.006%)。存活时间极短,在该病例中患者存活了12个月。使用CT扫描对畸形进行了描述。