Fryns J P, De Troch C, Van Mol C, Vandenbossche L
Centre for Human Genetics, University of Leuven, Belgium.
Clin Genet. 1996 Oct;50(4):212-6. doi: 10.1111/j.1399-0004.1996.tb02628.x.
In this report we describe two unrelated young males with severe mental retardation, persisting hypotonia, and constipation. A maternal uncle of one of these two boys died at the age of 18 months and presented the same clinical symptoms. The triad mental retardation, hypotonia, constipation is a characteristic finding in the FG syndrome, an X-linked mental retardation syndrome. At the present time, there is increasing evidence that the FG syndrome-phenotype may be present in different XLMR conditions, e.g. the fragile X syndrome. In addition to the triad severe mental retardation, hypotonia, constipation, the present two male index patients had a characteristic facial appearance with nasal hypoplasia, relative microcephaly and pre- and postnatal overgrowth. The question is raised whether the present two males are examples of a specific entity within the FG-syndrome-like phenotype.
在本报告中,我们描述了两名患有严重智力障碍、持续性肌张力减退和便秘的无血缘关系的年轻男性。这两名男孩中其中一人的一位舅舅在18个月大时死亡,且表现出相同的临床症状。智力障碍、肌张力减退、便秘三联征是FG综合征(一种X连锁智力障碍综合征)的典型表现。目前,越来越多的证据表明FG综合征表型可能存在于不同的X连锁智力障碍疾病中,例如脆性X综合征。除了严重智力障碍、肌张力减退、便秘三联征外,这两名男性索引患者还有特征性的面部外观,包括鼻发育不全、相对小头畸形以及出生前后生长过度。由此引发了一个问题,即这两名男性是否为例证,代表了FG综合征样表型中的一个特定实体。