Elite Clinical Laboratory

Introducing Our New Testing Services - Hereditary ENT Disorders Testing | Expanded Coverage: Now Serving More States - Call to know more.
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Hereditary ENT Disorders Risk Panel

Early detection of hereditary ENT conditions

Introduction

Genetic Insight into ENT Conditions

This panel identifies genetic variants associated with inherited disorders of the ears, nose, and throat—including multiple forms of hereditary hearing loss and craniofacial syndromes with ENT involvement. By uncovering the underlying cause of ENT-related symptoms, it supports early intervention, accurate diagnosis, and comprehensive care planning. It also provides valuable information for family counseling and future risk assessment in affected individuals and relatives.

Why the Test Is Significant​

Early Detection of Hearing Loss

Timely intervention, supporting speech & language development

Syndrome Identification Support

Guides multi-disciplinary care when ENT features are prominent

Progression Risk Insight

Assesses likelihood of worsening hearing over time

Family Genetic Awareness

Explains inheritance patterns and recurrence risks

Unknown and Interesting Facts

More than 50% of congenital hearing loss is linked to genetic causes. Many of these involve single-gene mutations that can present as isolated hearing issues or as part of a broader syndrome. For instance, genes associated with Usher syndrome affect both hearing and vision, while Alport syndrome impacts hearing and kidney function. Identifying the genetic cause not only clarifies the diagnosis but also helps predict progression and guides comprehensive care across affected organ systems, making early testing highly valuable.

Medical Necessity and Signs/Symptoms

  • Congenital or early-onset hearing loss
  • Family history of genetic ENT disorders
  • Syndromic features like facial or cranial anomalies
  • Inner ear balance problems or vestibular symptoms
  • Regressive or progressive hearing loss
  • Abnormal newborn hearing screening results
  • Suspected syndromes with ENT involvement (e.g., Usher, Pendred)
  • History of unexplained sensorineural hearing deficits

Post-Test Support

Elite Clinical Laboratory provides thorough post-test support with a focus on clarity and actionability. Our clinical team assists in interpreting genetic findings and facilitates access to genetic counselors with expertise in ENT-related conditions. We also help coordinate referrals to audiologists and otolaryngologists, ensuring that patients receive the multidisciplinary care required for complex hearing or craniofacial syndromes. Our goal is to support timely, informed intervention to optimize long-term outcomes.

Our Documentation