Heterozygous MYH9 Mutations in 2 Children With Cochlear Nerve Canal Stenosis.
Wenqi LiangLine WangWenrui ZhengShuguang HanKevin A PengPublished in: Ear, nose, & throat journal (2022)
MYH9 is a gene that encodes for a subunit of the myosin heavy chain IIA protein. Mutations in MYH9 are associated with hematologic abnormalities, renal dysfunction, and hearing loss. Bony cochlear nerve canal stenosis (CNCS), which is diagnosed on computed tomography (CT) imaging, has been associated with congenital deafness, cochlear nerve aplasia/hypoplasia, and inner ear malformations. We report two cases of CNCS presenting with profound congenital hearing loss whom we diagnosed with mutations in MYH9 and discuss the genotype-phenotype association and implications for management.
Keyphrases
- hearing loss
- hypertrophic cardiomyopathy
- computed tomography
- peripheral nerve
- left ventricular
- dual energy
- positron emission tomography
- image quality
- high resolution
- contrast enhanced
- magnetic resonance imaging
- binding protein
- genome wide
- case report
- amino acid
- magnetic resonance
- dna methylation
- mass spectrometry
- atrial fibrillation
- protein kinase