Flöttmann Ricarda, Sowinska-Seidler Anna, Lavie Julie, Chateil Jean-François, Lacombe Didier, Mundlos Stefan, Horn Denise, Spielmann Malte
Institute for Medical Genetics and Human Genetics, Charité Universitätsmedizin Berlin, Berlin, Germany.
Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
Eur J Hum Genet. 2016 Aug;24(8):1132-6. doi: 10.1038/ejhg.2015.266. Epub 2016 Jan 6.
Parathyroid hormone-like hormone (PTHLH, MIM 168470) plays an important role in endochondral bone development and prevents chondrocytes from differentiating. Disease-causing variants and haploinsufficiency of PTHLH are known to cause brachydactyly type E and short stature. So far, three large duplications encompassing several genes including PTHLH associating with enchondromatas and acro-osteolysis have been described in the literature. Here, we report on a three-generation pedigree with short humerus, curved radius, and a specific type of severe brachydactyly with features of types E and A1 but without the enchondromatas and the acro-osteolysis. Microarray-based comparative genomic hybridization (array-CGH) revealed a 70-kb duplication on chromosome 12p11.22 encompassing only PTHLH. Our data extend the phenotypic spectrum associated with copy number variations of PTHLH, and this family is to our knowledge the first description harboring a microduplication encompassing only PTHLH.
甲状旁腺激素样激素(PTHLH,MIM 168470)在软骨内骨发育中起重要作用,并阻止软骨细胞分化。已知PTHLH的致病变异和单倍体不足会导致E型短指症和身材矮小。迄今为止,文献中已描述了三个大型重复,其中包括几个与内生软骨瘤和肢端骨质溶解相关的基因,包括PTHLH。在此,我们报告了一个三代家系,其肱骨短、桡骨弯曲,以及一种特定类型的严重短指症,具有E型和A1型的特征,但没有内生软骨瘤和肢端骨质溶解。基于微阵列的比较基因组杂交(阵列CGH)显示12p11.22染色体上有一个70 kb的重复,仅包含PTHLH。我们的数据扩展了与PTHLH拷贝数变异相关的表型谱,据我们所知,这个家系是首个仅包含PTHLH微重复的描述。