Tatsi, Christina, Gkourogianni, Alexandra, Mohnike, Klaus, DeArment, Diana, Witchel, Selma, Andrade, Anenisia C., Markello, Thomas C., Baron, Jeffrey, Nilsson, Ola, Jee, Youn Hee, Tatsi, Christina, Gkourogianni, Alexandra, Mohnike, Klaus, DeArment, Diana, Witchel, Selma, Andrade, Anenisia C., Markello, Thomas C., Baron, Jeffrey, Nilsson, Ola, and Jee, Youn Hee
Aggrecan, a proteoglycan, is an important component of cartilage extracellular matrix, including that of the growth plate. Heterozygous mutations in ACAN, the gene encoding aggrecan, cause autosomal dominant short stature, accelerated skeletal maturation, and joint disease. The inheritance pattern and the presence of bone age equal to or greater than chronological age have been consistent features, serving as diagnostic clues. From family 1, a 6-year-old boy presented with short stature [height standard deviation score (SDS), -1.75] and bone age advanced by 3 years. There was no family history of short stature (height SDS: father, -0.76; mother, 0.7). Exome sequencing followed by Sanger sequencing identified a de novo novel heterozygous frameshift mutation in ACAN (c.6404delC: p.A2135Dfs). From family 2, a 12-year-old boy was evaluated for short stature (height SDS, -3.9). His bone age at the time of genetic evaluation was approximately 1 year less than his chronological age. Family history was consistent with an autosomal dominant inheritance of short stature, with several affected members also showing early-onset osteoarthritis. Exome sequencing, confirmed by Sanger sequencing, identified a novel nonsense mutation in ACAN (c.4852C>T: p.Q1618X), which cosegregated with the phenotype. In conclusion, patients with ACAN mutations may present with nonfamilial short stature and with bone age less than chronological age. These findings expand the known phenotypic spectrum of heterozygous ACAN mutations and indicate that this diagnosis should be considered in children without a family history of short stature and in children without accelerated skeletal maturation., Funding Agencies:Intramural Research Program, Eunice Kennedy Shriver National Institute of Child Health & Human Development, National Institutes of Health (NIH) Clinical Center Genomics Opportunity, NIH Intramural Research Program of the National Human Genome Research Institute Common Fund, Office of the Director, NIH Stockholm County Council Byggmästare Olle Engkvist Stiftelse Novo Nordisk Foundation NNF16OC0021508 Erik och Edith Fernström Foundation for Medical Research HKH Kronprinsessan Lovisas förening Karolinska Institutet, Stockholm, Sweden Örebro University, Örebro, Sweden