Recurrent Osteomyelitis in a Paediatric Patient with a Novel NTRK1 Mutation: A Case Report on Congenital Insensitivity to Pain with Anhidrosis
Through this case report, we aim to highlight the unique orthopaedic challenges encountered in the management of CIPA patients, emphasizing the importance of a multidisciplinary approach involving orthopaedic surgeons, paediatricians, geneticists, and physiotherapists. Additionally, we discuss the need for further research to elucidate optimal management strategies and improve outcomes in this rare and complex patient population.
Authors
- Dzintars Ozols (ORCID: https://orcid.org/0000-0002-2004-177X)
- Uldis Bergmanis
- Artūrs Vīksne
- Nityanand Jain (ORCID: https://orcid.org/0000-0002-7918-7909)
- M. Hassan Kakar (ORCID: https://orcid.org/0000-0001-5765-8207)
- Liena Gasiņa (ORCID: https://orcid.org/0000-0001-7401-6054)
Institutions
- Children's Clinical University Hospital (LV)
- Riga Stradiņš University (LV)
Publication Details
- Journal
- Children
- Published
- 2025-03-09
- DOI
- https://doi.org/10.3390/children12030344
- Primary Topic
- Hereditary Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00