# Role of Physiotherapy in Pediatric Lissencephaly: A Case Report and Therapeutic Insights

**Authors:** Anam R Sasun, H V Sharath

PMC · DOI: 10.7759/cureus.62901 · 2024-06-22

## TL;DR

This case report shows how physiotherapy can improve muscle tone and developmental milestones in a child with type 1 lissencephaly, a genetic disorder.

## Contribution

The study highlights the novel application of specific physiotherapy techniques in managing pediatric lissencephaly.

## Key findings

- Physiotherapy over 12 weeks improved muscle tone and developmental milestones in a child with type 1 lissencephaly.
- Techniques like Rood's approach and hippotherapy were effective in symptom management.
- The study emphasizes the importance of physiotherapy in improving quality of life for such patients.

## Abstract

Type 1 lissencephaly is a genetic disorder of chromosomal abnormality. This case report glimpses at the physiotherapy rehabilitation for a two-year-old male brought by his parents with complaints of being unable to move his upper and lower limbs, delayed milestones as compared to his peer group, and difficulty in swallowing. Physiotherapy rehabilitation included Rood's approach to neurodevelopmental techniques, hippotherapy, vestibular ball rehabilitation exercises, oral sensorimotor stimulation, and tactile stimulation. The protocol lasted for 12 weeks. At the end of the rehabilitation, there was a significant improvement in the tone of the muscles and delayed developmental milestones. Through this case report, we conclude about the importance of genetic counseling to the parents of genetic disorders babies. We ought to improve awareness about the pivotal role of physiotherapy in managing such disorders. We conclude that physiotherapy significantly improved the symptoms and improved the quality of life of patients with type 1 lissencephaly.

## Linked entities

- **Diseases:** lissencephaly (MONDO:0018838)

## Full-text entities

- **Diseases:** difficulty in (MESH:D051346), genetic disorder (MESH:D030342), chromosomal abnormality (MESH:D002869), Lissencephaly (MESH:D054082), Type 1 lissencephaly (MESH:D054221)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11262781/full.md

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Source: https://tomesphere.com/paper/PMC11262781