Radiological diagnosis of infantile osteopetrosis in a 1-year-old with macrocephaly and jaundice
Infantile osteopetrosis is a rare, severe genetic disorder marked by defective osteoclast function, leading to abnormally dense but fragile bones. Early diagnosis through radiologic imaging is essential for proper management, as it often reveals hallmark features such as diffuse skeletal sclerosis,...
Saved in:
Main Authors: | Aya Laridi, MD, Chaimaa Jabbari, MD, Ihssane Laasri, MD, Soufiane Hassar, MD, Nazik Allali, PhD, Latifa Chat, PhD, Siham El Haddad, PhD |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-09-01
|
Series: | Radiology Case Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1930043325004819 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clinical, genetic aspects and molecular pathogenesis of osteopetrosis
by: D. D. Nadyrshina, et al.
Published: (2023-07-01) -
Clinical features of infantile (malignant) osteopetrosis
by: E. L. Sahharovskaya, et al.
Published: (2022-11-01) -
Radiological features of malignant osteopetrosis at early and late stages of disease
by: E. L. Sakharovskaya, et al.
Published: (2014-07-01) -
Osteopetrosis and Hip Fracture. Case Report and Literature Review
by: Liyanira Alonso Leiva, et al.
Published: (2022-11-01) -
Osteopetrosis (marble bone disease)
by: Alexey Nikolayevich Kalyagin, et al.
Published: (2014-03-01)