Neri Caterina, Moser Karen, Pysher Theodore J, Boettger David R, Neri Giovanni, Opitz John M
Istituto di Ginecologia e Ostetricia, Università Cattolica del S. Cuore, Rome, Italy.
Fetal Pediatr Pathol. 2011;30(2):71-6. doi: 10.3109/15513815.2011.520259.
We report on a case of FG syndrome in an almost 6-year-old boy, diagnosed post-mortem. The description of the intellectual and behavior phenotype provided by the mother, together with the evidence gathered at autopsy, were sufficient to reach a clinical diagnosis. The mother had mild manifestations, including a symptomatic tethered cord, which established her as a carrier of the putative mutation causing the syndrome in the son. The propositus' phenotype did not suggest involvement of the MED12 gene.
我们报告了一例近6岁男孩的FG综合征病例,该病例为尸检后确诊。母亲提供的智力和行为表型描述,以及尸检收集的证据,足以做出临床诊断。母亲有轻度表现,包括有症状的脊髓拴系,这表明她是导致儿子患该综合征的推定突变的携带者。先证者的表型未提示MED12基因受累。