Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports

BACKGROUND: Hyaline fibromatosis syndrome is a rare progressive autosomal recessive connective tissue disorder caused by a mutation in the ANTXR2/CMG2 gene. According to its severity, patients may present with skin nodules or visceral infiltration, which carries a poor prognosis. Hypercalcemia has n...

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Detalles Bibliográficos
Autores principales: Ismail, Mariam M., Musa, Salwa A., Hassan, Samar S., Abdullah, Mohamed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236733/
https://www.ncbi.nlm.nih.gov/pubmed/37264371
http://dx.doi.org/10.1186/s13256-023-03927-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236733/
https://www.ncbi.nlm.nih.gov/pubmed/37264371
http://dx.doi.org/10.1186/s13256-023-03927-9

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