GTSF1

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  <title>GTSF1: A Rare Genetic Disorder with Profound Effects</title>
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<h1>GTSF1: A Rare Genetic Disorder with Profound Effects</h1>

<h2>Description</h2>

GTSF1 is a rare genetic disorder caused by mutations in the GTSF1 gene. This gene encodes a protein that is essential for the proper formation of the Golgi apparatus, a critical organelle responsible for protein trafficking and modification within cells.

GTSF1 deficiency leads to a range of developmental abnormalities, including:

* Skeletal malformations, such as scoliosis and kyphosis
* Intellectual disability
* Speech and language delay
* Vision and hearing problems
* Seizures
* Gastrointestinal issues

<h2>Associated Diseases</h2>

GTSF1 mutations have been linked to several specific diseases, including:

* <strong>Spondylocheiro dysostosis</strong>: A rare skeletal disorder characterized by short stature, curvature of the spine, and abnormal hands and feet.
* <strong>Gastrointestinal dysmotility</strong>: A condition that affects the movement of food and waste through the digestive tract.
* <strong>Retinitis pigmentosa</strong>: A degenerative eye disease that can lead to blindness.
* <strong>Sensorineural hearing loss</strong>: A type of hearing loss caused by damage to the inner ear.

**Did you Know ?**

GTSF1 is an extremely rare condition, affecting approximately 1 in 1 million people worldwide. However, it is believed that many cases go undiagnosed, as the symptoms can be subtle and variable.
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