Desai Hemina H, Patel Mahesh, Gonsai R N
Department of Pathology, BJ Medical College, Ahmedabad 380016.
J Indian Med Assoc. 2011 Sep;109(9):678.
Laurance Moon Bardet Biedl (LMBB) syndrome is a rare disorder characterised by retinitis pigmentosa, hexadactyly, obesity, mental retardation and hypogonadism. In the present case report the patient presented with the features of Laurence Moon Bardet Biedl syndrome in association with dyslipoproteinaemia.
劳伦斯-穆恩-巴德-比德尔(LMBB)综合征是一种罕见的疾病,其特征为色素性视网膜炎、多指(趾)畸形、肥胖、智力障碍和性腺功能减退。在本病例报告中,患者表现出劳伦斯-穆恩-巴德-比德尔综合征的特征,并伴有血脂蛋白异常血症。