CTGLF12P
CTGLF12P: The Gene Linked to Speech and Language Disorders
Description
CTGLF12P is a gene located on the human chromosome 6. It plays a crucial role in the development and function of the brain, particularly in areas responsible for speech and language. Mutations in this gene have been identified as a genetic cause of various speech and language disorders.
Associated Diseases
Mutations in CTGLF12P have been associated with the following speech and language disorders:
- Specific Language Impairment (SLI): A developmental disorder characterized by difficulties in acquiring and understanding language.
- Autism Spectrum Disorder (ASD): A neurodevelopmental condition that affects social interaction, communication, and behavior.
- Developmental Dyslexia: A learning disorder that impacts the ability to read, write, and spell.
- Speech Sound Disorders: Problems with producing certain speech sounds or combining them into words.
- Childhood Apraxia of Speech (CAS): A motor speech disorder that affects the ability to plan and coordinate speech movements.
Did you Know ?
According to the American Speech-Language-Hearing Association, approximately 1 in 10 children experience a speech or language disorder, making it one of the most common developmental challenges. Mutations in CTGLF12P are estimated to account for up to 10% of these disorders.
