SPANXN3
Title: The Enigmatic spanxn3 Gene: A Gateway to Understanding Rare Neurological Disorders
Description: The spanxn3 gene, an enigmatic entity in the vast realm of genetics, holds immense significance in shaping neurological functions. Its involvement in a rare and devastating spectrum of disorders, including microcephaly, intellectual disability, and autism, has brought it to the forefront of scientific research. This article delves into the intricate world of spanxn3, exploring its role in these debilitating conditions and showcasing the latest cutting-edge research unraveling its mysteries.
Associated Diseases:
Spanxn3 mutations have been implicated in the following rare neurological disorders:
- Microcephaly: Characterized by an unusually small head size due to impaired brain development.
- Intellectual Disability: A group of conditions that affect cognitive abilities, including learning, reasoning, and problem-solving.
- Autism Spectrum Disorder (ASD): A complex neurodevelopmental condition that affects social interactions, communication, and behavior.
Did you Know ?
- Microcephaly caused by spanxn3 mutations is estimated to affect approximately 1.5 in every 100,000 live births.
