Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
The documentation for autosomal recessive nonsyndromic hearing loss 93 is limited due to its rarity and the recent identification of its genetic basis. Conditions like this often lack extensive clinical studies because they affect a small population, making systematic research difficult. As awareness increases and more cases are identified, clinical characterization is expected to improve.
To navigate your care effectively, seek a specialist in genetic disorders, particularly one with experience in hearing loss and genetic deafness. Genetic counseling is highly recommended, as it can provide valuable insights into the implications of the CABP2 gene mutations for you and your family. You can find a genetic counselor through the National Society of Genetic Counselors at findageneticcounselor.com. Additionally, consider participating in any available clinical trials to contribute to research and potentially access new treatment options.
Currently, there is one active clinical trial related to autosomal recessive nonsyndromic hearing loss 93. This trial may provide insights into potential treatments or management strategies for individuals with this condition. For more information on this trial, you can visit ClinicalTrials.gov and search for 'autosomal recessive nonsyndromic hearing loss 93'.
Actionable guidance for navigating care for autosomal recessive nonsyndromic hearing loss 93
To navigate your care effectively, seek a specialist in genetic disorders, particularly one with experience in hearing loss and genetic deafness. Genetic counseling is highly recommended, as it can provide valuable insights into the implications of the CABP2 gene mutations for you and your family. You can find a genetic counselor through the National Society of Genetic Counselors at findageneticcounselor.com. Additionally, consider participating in any available clinical trials to contribute to research and potentially access new treatment options.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.