Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GSDME gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Inheritance patterns describe how genetic conditions are passed from parents to children.
Inheritance patterns describe how genetic conditions are passed from parents to children.
The documentation around autosomal dominant nonsyndromic hearing loss 5 is limited primarily due to its rarity and the recent identification of its genetic basis. As this condition affects a relatively small number of individuals, comprehensive clinical studies have not been extensively conducted, leading to gaps in understanding its full clinical picture.
To navigate your condition effectively, consider consulting with an audiologist who specializes in genetic hearing loss. Genetic counseling may also be beneficial, as it can provide insights into the implications of the GSDME mutation for you and your family. While there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can offer helpful information. Additionally, participating in clinical trials could provide access to new research and potential treatments.
Currently, there is one active clinical trial related to autosomal dominant nonsyndromic hearing loss 5. You can find more information about this trial and its details by visiting ClinicalTrials.gov at the following link: https://clinicaltrials.gov/search?cond=autosomal%20dominant%20nonsyndromic%20hearing%20loss%205. This trial may provide insights into potential future treatments or management strategies for this condition.
Actionable guidance for navigating care for autosomal dominant nonsyndromic hearing loss 5
To navigate your condition effectively, consider consulting with an audiologist who specializes in genetic hearing loss. Genetic counseling may also be beneficial, as it can provide insights into the implications of the GSDME mutation for you and your family. While there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can offer helpful information. Additionally, participating in clinical trials could provide access to new research and potential treatments.
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 6, 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.