Clinical and genetic characteristics of primary hypertrophic osteoarthropathy
Background. Primary hypertrophic osteoarthropathy is a rare genetically heterogeneous disease with three clinical variants. The classic one is a combination of hyperostosis, arthropathy and pachyderma and two variants with damage to only bone structures or pachyderma. Two genes responsible for the o...
Saved in:
| Main Authors: | E. L. Dadali, T. V. Markova, V. M. Kenis, T. S. Nagornova, S. S. Nikitin |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
ABV-press
2023-06-01
|
| Series: | Нервно-мышечные болезни |
| Subjects: | |
| Online Access: | https://nmb.abvpress.ru/jour/article/view/543 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Primary hypertrophic osteoarthropathy
by: E. L. Trisvetova
Published: (2020-11-01) -
Primary idiopathic hypertrophic osteoarthropathy in a child: characteristics of the disease with a case report
by: N. A. Lyubimova, et al.
Published: (2018-01-01) -
SECONDARY HYPERTROPHIC OSTEOARTHROPATHY (PIERRE MARIE–BAMBERGER SYNDROME)
by: A. S. Krylov, et al.
Published: (2017-10-01) -
Pachydermoperiostosis (Touraine-Solente-Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy
by: Fatima Khurshid, et al.
Published: (2025-03-01) -
Pachydermoperiostosis (Touraine-Solente-Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy
by: Fatima Khurshid, et al.
Published: (2025-03-01)