Fishman M A, Chang C S, Miller J E
Pediatrics. 1978 Apr;61(4):580-2.
Two patients with encephalocraniocutaneous lipomatosis have been studied. The main features of the syndrome are unilateral cutaneous and ophthalmologic lesions with ipsilateral cerebral malformations. Seizures beginning in infancy and varying degrees of mental retardation are present in affected patients. The involved tissues are derived from the embryonic ectodermal and mesodermal layers.
对两名患有脑颅皮肤脂肪瘤病的患者进行了研究。该综合征的主要特征是单侧皮肤和眼部病变以及同侧脑畸形。受影响的患者存在始于婴儿期的癫痫发作和不同程度的智力迟钝。受累组织源自胚胎外胚层和中胚层。
