# Case Report: Positioning head tilt observed in six dogs with meningoencephalitis of unknown origin

**Authors:** Shinji Tamura, Koen M. Santifort, Takayuki Kuwabara, Yuya Nakamoto, Yumiko Tamura

PMC · DOI: 10.3389/fvets.2026.1709307 · Frontiers in Veterinary Science · 2026-02-23

## TL;DR

This case report describes positioning head tilt in six dogs with meningoencephalitis of unknown origin, suggesting a possible link between the condition and this neurological sign.

## Contribution

The report adds to the understanding of positioning head tilt by documenting its occurrence in dogs with meningoencephalitis of unknown origin.

## Key findings

- Positioning head tilt was observed in six dogs diagnosed with meningoencephalitis of unknown origin.
- The exact causative lesion site could not be identified in these dogs.
- The findings suggest that meningoencephalitis of unknown origin may be a clinically relevant cause of positioning head tilt in dogs.

## Abstract

Positioning head tilt (PHT) is a dynamic clinical neurological sign that is characterized by a head tilt to the opposite side of a voluntary lateral turn of the head. Based on recent publications, various etiologies are proposed for the occurrence of PHT in dogs and cats. One suggested cause is a lack of inhibitory input to the vestibular nuclei due to dysfunction of the cerebellar nodulus and uvula (NU). In that category, it has been reported in dogs with hypoplasia of the NU, dogs with lysosomal storage diseases, and in a dog with a cerebellar tumor. Other proposed causes of PHT include reduced input of either proprioceptive information from the spindles of cervical muscles or information about head movement in space from peripheral vestibular apparatus. As examples of the former, it has been observed in feline cases of hypokalemic myopathy and myasthenia gravis. As an example of the latter, it has been observed in a dog and four cats with bilateral peripheral vestibular dysfunction. In this study, we describe and discuss our observations of PHT in six dogs with meningoencephalitis of unknown origin (MUO). Although it was not possible to identify the causative lesion site in these dogs, the possibility of MUO causing the clinical sign of PHT in dogs is deemed to be clinically relevant.

## Linked entities

- **Diseases:** myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Genes:** CSF2 (colony stimulating factor 2) [NCBI Gene 403923] {aka GM-CSF}
- **Diseases:** hypermetria (MESH:D002524), epileptic seizure (MESH:D004827), brain lesions (MESH:D001927), ataxia (MESH:D001259), consciousness (MESH:D003244), midbrain lesion (MESH:D020295), spinal cord syringomyelia (MESH:D013595), Pleocytosis (MESH:D007964), arachnoid diverticulum (MESH:D001100), hypokalemic myopathy (MESH:D009135), hepatitis (MESH:D056486), miosis (MESH:D015877), cerebellar herniation (MESH:D004677), anisocoria (MESH:D015875), NU dysfunction (MESH:C531732), cerebellar tumor (MESH:D002528), myasthenia gravis (MESH:D009157), meningoencephalitis (MESH:D008590), proprioceptive deficits (MESH:D020886), tumor (MESH:D009369), lysosomal disease (MESH:D016464), PHT (MESH:D006258), cerebellar hypoplasia (MESH:C562568), vestibular dysfunction (MESH:D015837), necrotic foci (MESH:C565785), tetraparesis (MESH:C565722), horizontal nystagmus (MESH:D009759), decreased level (MESH:C564133), cerebellar nodulus and uvula (MESH:D002526), MUO (MESH:D005335)
- **Chemicals:** MUO (-), prednisolone (MESH:D011239), cyclosporine (MESH:D016572), prednisone (MESH:D011241), cytarabine (MESH:D003561), phenobarbital (MESH:D010634)
- **Species:** Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12968010/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968010/full.md

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Source: https://tomesphere.com/paper/PMC12968010