Leegwater P A J, Boor P K I, Yuan B Q, van der Steen J, Visser A, Könst A A M, Oudejans C B M, Schutgens R B H, Pronk J C, van der Knaap M S
Department for Clinical Chemistry, Free University Medical Center, Amsterdam, The Netherlands.
Hum Genet. 2002 Mar;110(3):279-83. doi: 10.1007/s00439-002-0682-x. Epub 2002 Feb 8.
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is an inherited neurologic disorder with macrocephaly before the age of one and slowly progressive deterioration of motor functions. Magnetic resonance imaging shows diffusely abnormal and swollen white matter of the cerebral hemispheres and the presence of subcortical cysts in the anterior-temporal region and often also in the frontoparietal region. Mutations in the MLC1 gene, encoding a putative membrane protein, have been recently identified as a cause for MLC. Here, we describe 14 new mutations in 18 patients. Two identified polymorphisms lead to alterations of amino acid residues. The role, suggested by others, of a mutation in the MLC1gene in catatonic schizophrenia and the possible function of the MLC1 protein as a cation channel are discussed.
巨脑性白质脑病伴皮质下囊肿(MLC)是一种遗传性神经系统疾病,在1岁前出现巨头畸形,运动功能呈缓慢进行性恶化。磁共振成像显示大脑半球白质弥漫性异常肿胀,颞前区存在皮质下囊肿,额顶区也常出现。最近已确定,编码一种假定膜蛋白的MLC1基因突变是MLC的病因。在此,我们描述了18例患者中的14个新突变。两个已确定的多态性导致氨基酸残基改变。讨论了其他人提出的MLC1基因突变在紧张型精神分裂症中的作用以及MLC1蛋白作为阳离子通道的可能功能。