Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the EYA4 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 for autosomal dominant nonsyndromic hearing loss 10 is limited due to the rarity of the condition and the recent identification of its genetic basis. As fewer individuals are affected, systematic clinical studies have been challenging to conduct, resulting in a lack of comprehensive clinical characterization. This does not diminish the reality of your experience; rather, it highlights the ongoing need for research and understanding in this area.
To navigate your condition effectively, consider consulting with a geneticist or an otolaryngologist (ear, nose, and throat specialist) who has experience with hereditary hearing loss. Genetic counseling may also be beneficial to understand the implications of the EYA4 mutation for you and your family. While there are currently no specific patient organizations or registries identified for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support.
Actionable guidance for navigating care for autosomal dominant nonsyndromic hearing loss 10
To navigate your condition effectively, consider consulting with a geneticist or an otolaryngologist (ear, nose, and throat specialist) who has experience with hereditary hearing loss. Genetic counseling may also be beneficial to understand the implications of the EYA4 mutation for you and your family. While there are currently no specific patient organizations or registries identified for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support.
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.
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.