Hearing Loss Genetic Testing
Understanding Genetic Factors in Hearing Loss
Hearing loss may result from environmental, medical, or genetic factors. Inherited forms of deafness can affect single individuals or entire families and may be associated with other syndromes.
Our London-based hearing loss genetics service provides targeted genomic assessment to identify inherited causes, clarify recurrence risk, and guide reproductive planning.
Hearing Loss & Genetics Package – Who Is This Suitable For?
This package is designed for individuals and families seeking clarity regarding inherited hearing loss and reproductive risk. Both adult and paediatric patients are assessed with a consultant-led, personalised approach.
Individuals with hearing loss from birth or progressive impairment can benefit from targeted genomic testing to identify potential inherited causes.
Families with a known history of inherited deafness may seek assessment to understand recurrence risk and implications for future generations.
Patients with potential syndromic forms of hearing loss can receive genomic evaluation to clarify inheritance patterns and associated clinical features.
Couples considering pregnancy or IVF can benefit from understanding genetic risk, with guidance for reproductive decision-making and family cascade testing where relevant.
All patients receive a structured post-test consultation, ensuring personalised interpretation, clear guidance, and ongoing support for family planning decisions.
Comprehensive, consultant-led care. Our London hearing loss genetics service combines advanced genomic testing with personalised reproductive guidance, providing clarity and confidence for families.
What Does the Assessment Include?
1. Review of Audiology and Medical History
Comprehensive evaluation of audiology results, clinical records, and family pedigree to identify patterns suggesting genetic involvement.
2. Targeted Genomic Testing
Depending on clinical need, testing may include:
Comprehensive deafness panels
Whole Genome Sequencing (WGS) for complex cases
Analysis for syndromic associations
3. Reproductive Counselling
Assessment of inheritance patterns, recurrence risk, and guidance for family planning or prenatal options.
4. Structured Post-Test Consultation
Results are explained in a detailed session within four weeks, covering clinical interpretation, reproductive implications, and recommended next steps.
How Genetic Testing Supports Families
Genetic testing can:
Clarify the cause of hearing loss
Identify inheritance patterns (dominant, recessive, X-linked)
Inform reproductive decisions and IVF or donor considerations
Guide family cascade testing to assess at-risk relatives
Offer reassurance or early intervention strategies where appropriate
Our London-Based Hearing Loss Genetics Service
We offer a private, consultant-led service with the highest standards of confidentiality. Testing is conducted in accredited laboratories following UK regulatory guidelines. Collaboration with audiologists, ENT specialists, and paediatricians ensures integrated, multidisciplinary care for accurate results and personalised recommendations.
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Clarity, precision, and personalised care. Our London hearing loss genetics service ensures patients leave with clear understanding, confidence, and a plan tailored to their individual needs.
Dr Ehsan Karimiani
In this section you can check frequently asked questions.
Can genetic testing identify all causes of hearing loss?
While many inherited forms can be identified, some cases involve complex or multifactorial causes. Testing focuses on the most clinically relevant genes and syndromes.
Is testing suitable for children and adults?
Yes. Both adult and paediatric patients can undergo assessment, with tailored interpretation and counselling for each age group.
What is family cascade testing?
Family cascade testing involves evaluating at-risk relatives after a genetic variant is identified, helping families understand recurrence risk and reproductive options.
How long do results take?
Typically, results are available within four weeks, followed by a structured post-test consultation with a specialist.
Is reproductive counselling included?
Yes. Guidance on inheritance patterns, recurrence risk, and reproductive planning is provided as part of the package.
