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

BACKGROUND: 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 diagnosis cannot be made until pathology is completed after birth. Here, we pres...

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Detalles Bibliográficos
Autores principales: Lü, Yan, Jiang, Yulin, Wu, Huanwen, Qi, Qingwei, Zhou, Xiya, Guo, Qi, Hao, Na, Liu, Juntao, Meng, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416477/
https://www.ncbi.nlm.nih.gov/pubmed/37568122
http://dx.doi.org/10.1186/s12920-023-01612-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416477/
https://www.ncbi.nlm.nih.gov/pubmed/37568122
http://dx.doi.org/10.1186/s12920-023-01612-w

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