Multidisciplinary Center for CACNA1A-Related Disorders

Multidisciplinary Center for CACNA1A-Related Disorders

Welcome to the Multidisciplinary Center for CACNA1A-Related Disorders at UTHealth Houston, a premier facility that provides comprehensive care and innovative research for individuals affected by CACNA1A-related neurological and developmental disorders. We’re committed to improving quality of life for both children and adults through personalized care, community support, and cutting-edge research.

Have questions?

Welcome to the Multidisciplinary Center for CACNA1A-Related Disorders at UTHealth Houston, a premier facility that provides comprehensive care and innovative research for individuals affected by CACNA1A-related neurological and developmental disorders. We’re committed to improving quality of life for both children and adults through personalized care, community support, and cutting-edge research.

Our mission

The Multidisciplinary Center for CACNA1A-Related Disorders at UTHealth Houston is dedicated to delivering top-quality care and pioneering research to advance our understanding and treatment of CACNA1A-related disorders. Our goal is to enhance quality of life for all patients and families we serve.

About CACNA1A disorders

CACNA1A gene variants are associated with a spectrum of neurological conditions, including episodic ataxia, hemiplegic migraine, spinocerebellar ataxia, and developmental epileptic encephalopathies. While there is currently no cure, our growing understanding of these disorders informs treatment options and guides participation in clinical trials aimed at developing new therapies.

6410 Fannin St.

Suite 500 - Pediatric Care

Suite 1014 - Adult Care

Houston, TX 77030

Fax: (713) 486-9515

Parking available at the UTHealth Houston Garage, 6414 Fannin St.
Valet parking is also available.

How We Can Help

overlay

Personalized Care

Our multidisciplinary team of specialists provides tailored assessments and care plans to address each patient’s unique needs, ensuring the best possible outcomes.

overlay

Community Connection

We are proud to partner with the CACNA1A Foundation to provide resources, support, and opportunities for families to connect with others navigating similar diagnoses.

overlay

Genetic Testing and Counseling

Our genetic counselors guide you through the diagnosis of CACNA1A-related disorders, helping you understand its medical, psychosocial, and familial implications. In collaboration with leading genetics research experts, they also offer personalized insights into each patient’s CACNA1A variant.

overlay

Research Participation

Our research aims to:

  • Understand how genetic changes contribute to epilepsy and the spectrum of CACNA1A-related disorders.
  • Test the effectiveness of various new treatments.
  • Develop new tools to predict how the disease will progress and respond to treatment.
  • Utilize the latest wearable technology to collect biological data, such as heart rate, blood oxygen levels, and respiratory rate, to investigate possible biomarkers for CACNA1A-related disorders.

Request additional information

"*" indicates required fields

Name*
This field is for validation purposes and should be left unchanged.