Unilateral Referral on Newborn Hearing Screening, What if It is IP-II? A Case Report

Sule Cekic1, Gulsum Aydan Genc2, Levent Sennaroglu3

  • 1Audiology Department, Ankara Yildirim Beyazit University, Ankara, Turkey.

Insights

This case report highlights the importance of follow-up for infants with failed newborn hearing screening. Early diagnosis and intervention are crucial for managing progressive hearing loss in children with Ichthyosis Preauricular Type II (IP-II).

Area of Science:

  • Otolaryngology
  • Genetics
  • Pediatrics

Background:

  • Ichthyosis Preauricular Type II (IP-II) is a rare genetic disorder.
  • Children with IP-II may present with hearing impairments.
  • Newborn hearing screening is critical for early detection of hearing loss.

Purpose of the Study:

  • To present a case of bilateral IP-II with unilateral failed newborn hearing screening.
  • To demonstrate the diagnostic and intervention processes for progressive hearing loss in a child with IP-II.
  • To emphasize the significance of follow-up and auditory intervention.

Main Methods:

  • Case report methodology.
  • Diagnostic evaluation included pure tone audiometry, Auditory Brainstem Response (ABR), and Magnetic Resonance Imaging (MRI).
  • Management involved radiological assessment, hearing intervention, and follow-up.

Main Results:

  • A 6-year-old boy diagnosed with bilateral IP-II and progressive hearing loss.
  • Radiological imaging confirmed IP-II and aided in diagnosis.
  • Auditory intervention was necessary due to the child's hearing needs.

Conclusions:

  • Follow-up of referred children from newborn hearing screening is essential.
  • Radiological imaging plays a vital role in diagnosing and managing hearing loss.
  • Addressing progressive hearing loss and providing auditory intervention is crucial for developmental outcomes.