Sarker U K, Roy N, Roy J, Chakrabarty R, Bhattacharjee M
Dr Uttam Kumar Sarker, Assistant Professor, Department of Neurology, Mymensingh Medical College (MMC), Mymensingh, Bangladesh; E-mail:
Mymensingh Med J. 2019 Apr;28(2):456-460.
Sturge Weber Syndrome (SWS) is a sporadic neurocutanous disease characterized by facial port wine stain, ocular abnormalities and leptomengealangioma. We present here a 20 year old normotensive, non-diabetic lady hailing from Sarishabari, Jamalur District, Bangladesh got admitted in Mymensingh Medical College Hospital (MMCH), Mymensingh, Bangladesh on 15 July 2018 with the complaints of recurrent convulsion since 3 months of her life, weakness of the right side of the body for same duration according to the statement of the patients mother she was reasonably well until 3 months of her age. The precise pathogenesis is unknown. Clinical feature vary from gentle to full blown sickness with facial stain, seizures and glaucoma.
斯特奇-韦伯综合征(SWS)是一种散发性神经皮肤疾病,其特征为面部葡萄酒色斑、眼部异常和软脑膜血管瘤。我们在此介绍一位20岁的血压正常、非糖尿病女性,她来自孟加拉国贾马卢尔区萨里沙巴里,于2018年7月15日入住孟加拉国迈门辛医学院医院(MMCH),迈门辛。据患者母亲称,自出生3个月以来,她一直反复惊厥,身体右侧无力,持续时间相同。在3个月大之前,她一直状况良好。确切的发病机制尚不清楚。临床特征从轻微到严重不等,包括面部色斑、癫痫发作和青光眼。