Table 2 Genetic data of children with neurocristopathy-related hearing loss.

From: Analysis of the clinical features of neurocristopathy-related hearing loss and how these relate to outcomes after cochlear implantation

ID

Gene mutation

WS01

EDN3, MYO15A

WS02

SOX10

WS03

EDNRB

WS04

EDN3

WS05

EDNRB

WS06

SOX10

NS01

PTPN11

NS02

PTPN11

NS03

PTPN11, PKP2

KS01

KMT2D

CS01

CHD7

CS02

CHD7

CS03

CHD7

CS04

CHD7

CS05

CHD7

CS06

CHD7

  1. CS: CHARGE syndrome, ID: identification number, KS: Kabuki syndrome, NS: Noonan syndrome, WS: Waardenburg syndrome.
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