Dobyns W B, Berry-Kravis E, Havernick N J, Holden K R, Viskochil D
Departments of Human Genetics, Neurology, and Pediatrics, The University of Chicago, Chicago, Illinois 60637, USA.
Am J Med Genet. 1999 Oct 8;86(4):331-7.
Lissencephaly has been described in over 10 distinct malformation syndromes. Recently, we have recognized 5 children from four unrelated families with an almost identical disorder comprising lissencephaly with a posterior-to-anterior gradient and only moderate increase in thickness of the cortex, absent corpus callosum, neonatal-onset epilepsy, hypothalamic dysfunction including deficient temperature regulation, and ambiguous genitalia in genotypic males. Our observation of 5 affected males in one of these families is consistent with an X-linked pattern of inheritance. However, it differs in many regards from the X-linked form of isolated lissencephaly sequence that is associated with mutations of the XLIS (DCX) gene. Therefore, we propose that this disorder comprises a new X-linked malformation syndrome, which we refer to as X-linked lissencephaly with ambiguous genitalia (XLA-G).
无脑回畸形已在超过10种不同的畸形综合征中被描述。最近,我们从四个无亲缘关系的家庭中识别出5名儿童,他们患有几乎相同的疾病,包括具有从后向前梯度的无脑回畸形且皮质厚度仅适度增加、胼胝体缺失、新生儿期癫痫发作、下丘脑功能障碍(包括体温调节缺陷)以及基因型为男性者存在生殖器模糊。我们在其中一个家庭中观察到5名患病男性,这与X连锁遗传模式相符。然而,它在许多方面与与XLIS(DCX)基因突变相关的孤立性无脑回序列的X连锁形式不同。因此,我们提出这种疾病构成一种新的X连锁畸形综合征,我们将其称为伴有生殖器模糊的X连锁无脑回畸形(XLA-G)。