Ribbing disease
A hereditary disorder characterized by progressive thickening and SCLEROSIS of the DIAPHYSES causing pain and swelling of lesions. In contrast to Camurati-Engelmann Syndrome, it is likely autosomal recessive in its inheritance pattern, tends to unilaterally or asymmetrically affect only the limbs, and has a later age of onset. OMIM: 601477
Also Known As:
Diaphyseal sclerosis, multiple; Hereditary multiple diaphyseal sclerosis; Multiple diaphyseal sclerosis
Networked: 5
relevant articles (0 outcomes,
1 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Cai, Yangting:
1 article
(08/2018)
|
2. | Huang, Feng:
1 article
(08/2018)
|
3. | Huang, Yaohua:
1 article
(08/2018)
|
4. | Lin, Haixiong:
1 article
(08/2018)
|
5. | Zhang, Shuncong:
1 article
(08/2018)
|
6. | Zheng, Xiaohui:
1 article
(08/2018)
|
7. | Carotti, M:
1 article
(10/2016)
|
8. | Di Carlo, M:
1 article
(10/2016)
|
9. | Salaffi, F:
1 article
(10/2016)
|
10. | Silveri, F:
1 article
(10/2016)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Ribbing disease: