Leichtman L G, Wood B, Rohn R
Department of Pediatrics, Eastern Virginia Medical School, Norfolk 23501-1980.
Am J Med Genet. 1994 Mar 1;50(1):39-41. doi: 10.1002/ajmg.1320500108.
We describe an infant with a unique pattern of midline defects, including anophthalmia, cleft lip and palate, macrocephaly, cutis aplasia, and micrognathia. CNS anomalies including massive hydrocephalus with destruction of most recognizable structures were observed. The infant also developed panhypopituitarism, diabetes insipidus, and a seizure disorder. We postulate that this patient could represent a more complex form of the Delleman syndrome or a new morphogenetic syndrome secondary to ventral induction with extension to the developmental fields of the first and second branchial arches.
我们描述了一名患有独特中线缺陷模式的婴儿,包括无眼畸形、唇腭裂、巨头畸形、皮肤发育不全和小颌畸形。观察到中枢神经系统异常,包括伴有大多数可识别结构破坏的大量脑积水。该婴儿还出现了全垂体功能减退、尿崩症和癫痫发作障碍。我们推测,这名患者可能代表了一种更复杂形式的德耳曼综合征,或继发于腹侧诱导并扩展至第一和第二鳃弓发育区域的一种新的形态发生综合征。