Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review

Infantile myofibromatosis (IM) is a rare disorder characterized by the formation of nodules in the skin, muscle, bone, and, more rarely, visceral organs. Very few cases are detected prenatally, and the final d...

Source: BMC Medical Genomics - August 11, 2023 Category: Genetics & Stem Cells Authors: Yan L ü, Yulin Jiang, Huanwen Wu, Qingwei Qi, Xiya Zhou, Qi Guo, Na Hao, Juntao Liu and Hua Meng Tags: Case report Source Type: research