The diagnostic challenge of juvenile hyaline fibromatosis, a case report with literature reviews

INTRODUCTION: Juvenile hyaline fibromatosis (JHF) is a rare genetic condition characterized by impaired collagen production or metabolism. This study aims to present a rare case of JHF. CASE REPORT: An 11-year-old boy presented with bilateral keloid-like lesions on his ears and admitted intermittent...

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Detalles Bibliográficos
Autores principales: Ahmed, Ronak S., Ali, Alaa A., Abdullah, Hiwa O., Abdullah, Ari M., Naqar, Sharo, Salih, Abdulwahid M., Fatah, Mariwan L., Kakamad, Fahmi H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927703/
https://www.ncbi.nlm.nih.gov/pubmed/35303606
http://dx.doi.org/10.1016/j.ijscr.2022.106897

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927703/
https://www.ncbi.nlm.nih.gov/pubmed/35303606
http://dx.doi.org/10.1016/j.ijscr.2022.106897

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