Imaging manifestations of juvenile hyaline fibromatosis: a case report and literature review

OBJECTIVE: Juvenile hyaline fibromatosis (JHF) is an autosomal recessive condition caused by a mutation in capillary morphogenesis gene 2 (CMG2) on chromosome 4q21. JHF is an extremely rare genetic disorder, and fewer than a hundred cases have been reported worldwide. In this case report, the clinic...

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Detalles Bibliográficos
Autores principales: Yu, Jinfen, Wang, Linsheng, Tian, Jing, Yu, Xuewen, Sun, Lixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461728/
https://www.ncbi.nlm.nih.gov/pubmed/36101737
http://dx.doi.org/10.1259/bjrcr.20210167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461728/
https://www.ncbi.nlm.nih.gov/pubmed/36101737
http://dx.doi.org/10.1259/bjrcr.20210167

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