# Spine surgery and complication in familial dysautonomia: a case report

**Authors:** M. Fava, G. Ciani, R. Ghermandi, C. Cini, B. Maccaferri, A. Gasbarrini

PMC · DOI: 10.3389/fsurg.2025.1559346 · 2025-06-18

## TL;DR

This paper reports a case of a patient with familial dysautonomia who had multiple spinal surgeries, offering insights into managing this rare condition.

## Contribution

The study provides a detailed case report to guide the management of spinal issues in familial dysautonomia patients.

## Key findings

- FD patients have a higher risk of kyphoscoliosis and osteomyelitis.
- Spinal surgery in FD patients requires careful management due to multiple comorbidities.
- Sharing this case may help improve treatment strategies for FD-related vertebral pathologies.

## Abstract

Familial dysautonomia (FD) is an inherited severe congenital disease and a rare syndrome associated with progressive neuronal degeneration throughout life. Among its orthopedic conditions, FD patients have an higher incidence of kyphoscoliosis and osteomyelitis. Due to the rarity of FD and the presence of multiple comorbidities, there are currently no established guidelines for the management of vertebral pathologies associated with FD. Hence, this highlights the importance of sharing the case of our patient. The purpose of our study is to report the case of a 45-year-old patient with FD who underwent multiple spinal surgeries at our clinic, to provide possible indications for the most effective management of this rare condition.

## Linked entities

- **Diseases:** familial dysautonomia (MONDO:0009131), osteomyelitis (MONDO:0005246)

## Full-text entities

- **Diseases:** FD (MESH:D004402), neuronal degeneration (MESH:D009410), osteomyelitis (MESH:D010019), kyphoscoliosis (MESH:C565711), congenital disease (MESH:D030342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12213804/full.md

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Source: https://tomesphere.com/paper/PMC12213804