Budny Bartlomiej, Chen Wei, Omran Heymut, Fliegauf Manfred, Tzschach Andreas, Wisniewska Marzena, Jensen Lars R, Raynaud Martine, Shoichet Sarah A, Badura Magda, Lenzner Steffen, Latos-Bielenska Anna, Ropers Hans-Hilger
Max Planck Institute for Molecular Genetics, Ihnestr. 73, 14195, Berlin, Germany.
Hum Genet. 2006 Sep;120(2):171-8. doi: 10.1007/s00439-006-0210-5. Epub 2006 Jun 17.
We report on a large family in which a novel X-linked recessive mental retardation (XLMR) syndrome comprising macrocephaly and ciliary dysfunction co-segregates with a frameshift mutation in the OFD1 gene. Mutations of OFD1 have been associated with oral-facial-digital type 1 syndrome (OFD1S) that is characterized by X-chromosomal dominant inheritance and lethality in males. In contrast, the carrier females of our family were clinically inconspicuous, and the affected males suffered from severe mental retardation, recurrent respiratory tract infections and macrocephaly. All but one of the affected males died from respiratory problems in infancy; and impaired ciliary motility was confirmed in the index patient by high-speed video microscopy examination of nasal epithelium. This family broadens the phenotypic spectrum of OFD1 mutations in an unexpected way and sheds light on the complexity of the underlying disease mechanisms.
我们报告了一个大家庭,其中一种包含巨头畸形和纤毛功能障碍的新型X连锁隐性智力迟钝(XLMR)综合征与OFD1基因中的移码突变共同分离。OFD1的突变与口面指综合征1型(OFD1S)相关,该综合征以X染色体显性遗传和男性致死率为特征。相比之下,我们家系的携带者女性在临床上并无明显症状,而受影响的男性则患有严重智力迟钝、反复呼吸道感染和巨头畸形。除一名受影响男性外,其他所有男性均在婴儿期死于呼吸问题;通过对鼻上皮进行高速视频显微镜检查,在索引患者中证实了纤毛运动受损。这个家系以意想不到的方式拓宽了OFD1突变的表型谱,并揭示了潜在疾病机制的复杂性。