Prenatal diagnosis of a novel pathogenic variation in the ACAN gene presenting with isolated shortening of fetal long bones in the second trimester of gestation: a case report

Abstract Background Heterozygous mutations of the ACAN gene are a major cause of different evolutive growth defects in the pediatric population, but were never described as a cause of fetal skeletal dysplasia. Case presentation A G1 at 21w + 3d came to our institution for the second-trimester ultras...

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Principais autores:	Paolo Toscano, Lavinia Di Meglio, Fortunato Lonardo, Letizia Di Meglio, Laura Letizia Mazzarelli, Carmine Sica, Aniello Di Meglio
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BMC 2021-06-01
סדרה:	BMC Pregnancy and Childbirth
נושאים:	Prenatal diagnosis Skeletal dysplasia ACAN Aggrecan Case report
גישה מקוונת:	https://doi.org/10.1186/s12884-021-03952-w
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