Genetic mutation susceptibility of hearing loss in child with severe neonatal jaundice

Farah Dayana Zahedi, Abdul Rahman Roslenda, Adli Ali, Asma Abdullah

Research output: Contribution to journalArticle

Abstract

We report a case of 5-year-old boy who had bilateral profound sensorineural hearing loss His other two elder brothers have bilateral sensorineural hearing loss and history of severe neonatal jaundice as well. CT scan and MRI revealed normal findings. Right sided cochlear implantation was done at the age of 3 and he is still under audiology follow-up.

Original languageEnglish
Pages (from-to)477-479
Number of pages3
JournalRawal Medical Journal
Volume40
Issue number4
Publication statusPublished - 1 Oct 2015

Fingerprint

Neonatal Jaundice
Sensorineural Hearing Loss
Genetic Predisposition to Disease
Hearing Loss
Bilateral Hearing Loss
Audiology
Cochlear Implantation
Mutation
Siblings
Magnetic Resonance Imaging

Keywords

  • Congenital
  • Hearing loss
  • Hyperbilirubinemia
  • Jaundice

ASJC Scopus subject areas

  • Medicine(all)
  • Nursing(all)

Cite this

Genetic mutation susceptibility of hearing loss in child with severe neonatal jaundice. / Zahedi, Farah Dayana; Roslenda, Abdul Rahman; Ali, Adli; Abdullah, Asma.

In: Rawal Medical Journal, Vol. 40, No. 4, 01.10.2015, p. 477-479.

Research output: Contribution to journalArticle

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