Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOA 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.
Documentation for autosomal recessive nonsyndromic hearing loss 22 is limited primarily due to its rarity and the recent identification of the OTOA gene's role in the condition. As this condition affects a small number of individuals, systematic clinical studies have not been extensively conducted. This makes comprehensive clinical characterization challenging, but ongoing research may provide more insights in the future.
To navigate autosomal recessive nonsyndromic hearing loss 22, consider consulting with a geneticist or an audiologist specializing in hereditary hearing disorders. Genetic counseling is recommended to understand the implications of the OTOA gene mutation for family members and potential testing options. While there are currently no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Engaging with a genetic counselor can help you explore testing and family planning options.
Actionable guidance for navigating care for autosomal recessive nonsyndromic hearing loss 22
To navigate autosomal recessive nonsyndromic hearing loss 22, consider consulting with a geneticist or an audiologist specializing in hereditary hearing disorders. Genetic counseling is recommended to understand the implications of the OTOA gene mutation for family members and potential testing options. While there are currently no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Engaging with a genetic counselor can help you explore testing and family planning 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.
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.
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