Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutation.

International journal of pediatric otorhinolaryngology - 1 Dec 2016

Wester Jacob L, Merna Catherine, Peng Kevin A, Lewis Rebecca, Sepahdari Ali R, Ishiyama Gail, Hosokawa Kumiko, Kumakawa Kozo, Ishiyama Akira

Abstract excerpt

We report a case of a nine-year-old male who presented with facial nerve stimulation four years after cochlear implantation. Computed tomography was performed revealing a dilated internal auditory meatus and the cochlear implant electrode was found to be protruding into the fallopian canal at the level of the geniculate ganglion. Subsequent genetic analysis demonstrated X-linked deafness type 2 (DFNX2) caused by...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Cochlear Implants

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electric Stimulation

Share to Genetic Diseases, X-Linked

Share to Hearing Loss, Conductive

Share to Hearing Loss, Sensorineural

Share to Mutation

Source

Identifiers

PMID: 27863625
DOI: 10.1016/j.ijporl.2016.10.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutation.PMID 27863625Read ↗

Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.Semantic proximity Read ↗

X-linked Gusher Disease DFNX2 in Children, a Rare Inner Ear Dysplasia with Conductive Hearing LossSemantic proximity Read ↗

Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.Semantic proximity Read ↗

X-linked Malformation and Cochlear Implantation.Semantic proximity Read ↗

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child With X-Linked Deafness.Semantic proximity Read ↗

Research progress on incomplete partition type 3 inner ear malformation.Semantic proximity Read ↗

A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.Semantic proximity Read ↗

Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation.Semantic proximity Read ↗

Deletion of and Novel Missense Mutation in POU3F4 in 2 Families Segregating X-Linked Nonsyndromic DeafnessSemantic proximity Read ↗

HRCT and MRI findings in X-linked non-syndromic deafness patients with a POU3F4 mutation.Semantic proximity Read ↗

[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)].Semantic proximity Read ↗

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.