Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MSRB3 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 recessive nonsyndromic hearing loss 74 is limited because this condition affects a small number of individuals, which restricts the availability of systematic clinical studies. Additionally, the genetic basis was only recently identified, and ongoing clinical characterization is needed to better understand its full impact.
To navigate your path forward, consider seeking a geneticist or an audiologist with expertise in hereditary hearing loss. Genetic counseling is recommended to discuss the implications of the MSRB3 gene mutation for you and your family. While there are currently no patient organizations specifically for this condition, you can find resources through the Genetic and Rare Diseases Information Center at rarediseases.info.nih.gov. Additionally, consider looking into local hearing loss support groups for community and resources.
Actionable guidance for navigating care for autosomal recessive nonsyndromic hearing loss 74
To navigate your path forward, consider seeking a geneticist or an audiologist with expertise in hereditary hearing loss. Genetic counseling is recommended to discuss the implications of the MSRB3 gene mutation for you and your family. While there are currently no patient organizations specifically for this condition, you can find resources through the Genetic and Rare Diseases Information Center at rarediseases.info.nih.gov. Additionally, consider looking into local hearing loss support groups for community and resources.
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.