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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...
Autores principales: | Yu, Jinfen, Wang, Linsheng, Tian, Jing, Yu, Xuewen, Sun, Lixin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Institute of Radiology.
2022
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Materias: | |
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 |
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