Claes S, Devriendt K, Lagae L, Ceulemans B, Dom L, Casaer P, Raeymaekers P, Cassiman J J, Fryns J P
Center for Human Genetics, University of Leuven, Belgium.
Ann Neurol. 1997 Sep;42(3):360-4. doi: 10.1002/ana.410420313.
We report 2 families with X-linked infantile spasms syndrome (X-linked West syndrome). Data from clinical examination, biochemical analysis, neuroimaging, and neuropathology are discussed. In these families, genetic linkage analysis was able to locate the disease gene to the distal part of the short arm of the X chromosome, between Xpter and Xp11.4. This is the first report of linkage with genetic markers in this disorder. Although most cases are sporadic, further unraveling of the genetic background of the familial cases might greatly improve our understanding of infantile spasms.
我们报告了2个患有X连锁婴儿痉挛综合征(X连锁韦斯特综合征)的家族。讨论了来自临床检查、生化分析、神经影像学和神经病理学的数据。在这些家族中,遗传连锁分析能够将疾病基因定位到X染色体短臂的远端,位于Xpter和Xp11.4之间。这是该疾病与遗传标记连锁的首次报告。尽管大多数病例是散发性的,但对家族性病例遗传背景的进一步阐明可能会极大地增进我们对婴儿痉挛的理解。