Singh Ankur, Cuevas-Covarrubias Sergio, Pradhan Gaurav, Gautam V K, Messina-Baas Olga, Gonzalez-Huerta Luz Maria, Goyal Manisha, Kapoor Seema
Department of Pediatrics, LHMC and associated Kalawati Saran Children Hospital, New Delhi, India.
Indian J Pediatr. 2015 May;82(5):471-3. doi: 10.1007/s12098-014-1582-5. Epub 2014 Oct 12.
Pycnodysostosis (OMIM # 265800) is an inherited lysosomal disorder due to affection of cathepsin K gene, localised to 1q21. Pycnodysostosis can present with both skeletal and extraskeletal features. The index patient presented with cardinal features of short stature, dental and digital anomalies with history of multiple fractures. He, in addition had an unreported finding of white matter hyperintensity suggesting dysmyelination on neuroimaging. Molecular analysis revealed a homozygous insertion of single nucleotide in exon 5 of the CTSK gene that produces the substitution of phenylalanine instead of leucine at position 160 of protein and a premature termination of protein synthesis due to insertion of a stop codon. This mutation (c.480_481insT), (p.L160fsX173) is a novel frameshift mutation. The index case extends the phenotypic spectrum and the list of previously reported mutations in the CTSK gene.
致密性成骨不全症(OMIM # 265800)是一种由于组织蛋白酶K基因受影响而导致的遗传性溶酶体疾病,该基因定位于1q21。致密性成骨不全症可表现出骨骼和骨骼外的特征。索引患者表现出身材矮小、牙齿和手指异常以及多处骨折病史等主要特征。此外,他还有一项未报告的发现,即神经影像学显示白质高信号,提示髓鞘形成异常。分子分析显示,CTSK基因外显子5中存在单核苷酸纯合插入,导致蛋白质第160位的苯丙氨酸取代了亮氨酸,并且由于插入终止密码子而导致蛋白质合成提前终止。这种突变(c.480_481insT),(p.L160fsX173)是一种新的移码突变。索引病例扩展了CTSK基因的表型谱和先前报道的突变列表。