Craniofacial fibrous dysplasia: case report of uncommon genetic defect in young adult

Fibrous dysplasia is uncommon genetic defect in which normal bone and marrow are replaced with fibro-osseous tissue, leading to bone deformities, pain fractures and functional impairments. The case presents 27 years old women that was diagnosed with sepsis in the course of catheter-related infection...

Full description

Saved in:
Bibliographic Details
Main Authors: Konrad Haraziński, Weronika Goliat, Oliwia Sysło, Izabela Jastrzębska, Nikola Rubik, Maksym Gmur, Michał Gajewski, Barbara Sławińska, Zuzanna Błecha, Nicole Maryniak
Format: Article
Language:English
Published: Kazimierz Wielki University 2025-05-01
Series:Journal of Education, Health and Sport
Subjects:
Online Access:https://apcz.umk.pl/JEHS/article/view/59957
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Fibrous dysplasia is uncommon genetic defect in which normal bone and marrow are replaced with fibro-osseous tissue, leading to bone deformities, pain fractures and functional impairments. The case presents 27 years old women that was diagnosed with sepsis in the course of catheter-related infection and treated at nephrology department. She was diagnosed with chronic kidney disease that started during pregnancy and originated due to steroid-resistant nephrotic syndrome. During the hospitalization, a CT scan of the head was performed because of facial deformation. Based on CT scans of head, craniofacial fibrous dysplasia was confirmed.
ISSN:2391-8306