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Bilateral Hearing Loss in a Pallister–Killian Syndrome Patient

Year: 2025

Type: article

Abstract: Pallister–Killian syndrome (PKS) is a rare genetic disorder with multidisciplinary involvement caused by mosaic tetrasomy of the short arm of chromosome 12 (12p). The audiological findings obtained in patients with PKS have been limited in the literature. This report describes a 17-month-old boy with mixed hearing loss presented with PKS. Due to multiple systemic abnormalities seen in individuals with PKS, individuals with suspected hearing loss should be included in the amplification and rehabilitation process with early diagnosis.

Source: Indian Journal of Otology

DOI: 10.4103/indianjotol.indianjotol_98_24

Authors: Aysenur Aykul Yagcioglu, Merve Ozses, Betul Cicek Cinar

Institutions: KTO Karatay University, Hacettepe University

Language: English

Topic: Hearing Loss and Rehabilitation

Subfield: Cognitive Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: hybrid

OpenAlex ID: W4411516730

FWCI:

Cites: 13

Cited by:

Related to: 10