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.

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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
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article

Recurrent Osteomyelitis in a Paediatric Patient with a Novel NTRK1 Mutation: A Case Report on Congenital Insensitivity to Pain with Anhidrosis

Dzintars Ozols, Uldis Bergmanis, Artūrs Vīksne, Nityanand Jain et al.
Children
Hereditary Neurological Disorders
article

Recurrent Osteomyelitis in a Paediatric Patient with a Novel NTRK1 Mutation: A Case Report on Congenital Insensitivity to Pain with Anhidrosis

Dzintars Ozols, Uldis Bergmanis, Artūrs Vīksne, Nityanand Jain, M. Hassan Kakar, Liena Gasiņa
article en

Abstract

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.

ChildrenVol. 12(3)
Children's Clinical University Hospital (LV), Riga Stradiņš University (LV)
Good health and well-being
Openalex Percentile: Top 95%
Hereditary Neurological Disorders
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