Department of Paediatrics and Child Health, Dunedin School of Medicine, Otago University, Dunedin, New Zealand.
Am J Med Genet A. 2011 Dec;155A(12):3144-7. doi: 10.1002/ajmg.a.34311. Epub 2011 Nov 3.
We report on a follow-up evaluation of a male with a phenotype including craniosynostosis, periventricular nodular heterotopia, and neurodevelopmental delay. He was initially assigned a clinical diagnosis of Fontaine-Farriaux syndrome (FFS) as an infant although now, with improved delineation of this entity, it is evident that this diagnosis is not applicable to this individual. Array comparative genomic hybridization has demonstrated a 300 kb interstitial deletion on Xp22.11 affecting all or part of three annotated genes, ZFX, PDK3, and PCYT1B in this subject. The deletion was inherited from the phenotypically normal mother who also exhibited markedly skewed X-inactivation. These findings implicate hemizygosity for one or all three of these genes as the cause of this phenotype.
我们报告了一名男性患者的随访评估结果,其表型包括颅缝早闭、脑室周围结节性异位和神经发育迟缓。他在婴儿时期被初步诊断为 Fontaine-Farriaux 综合征(FFS),尽管现在随着对该疾病的认识的提高,很明显这个诊断不适用于该患者。阵列比较基因组杂交显示,Xp22.11 上有一个 300kb 的染色体间缺失,影响了三个注释基因 ZFX、PDK3 和 PCYT1B 的全部或部分。该缺失是从表型正常的母亲那里遗传而来的,母亲也表现出明显的 X 染色体失活偏倚。这些发现提示这些基因中的一个或全部三个基因的半合子缺失是导致该表型的原因。