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Postlingual sensorineural hearing impairment

MedGen UID:
870217
Concept ID:
C4024654
Pathologic Function
HPO: HP:0008596

Definition

A form of sensorineural hearing impairment with onset after the acquisition of speech. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVPostlingual sensorineural hearing impairment

Conditions with this feature

Deafness dystonia syndrome
MedGen UID:
162903
Concept ID:
C0796074
Disease or Syndrome
Males with deafness-dystonia-optic neuronopathy (DDON) syndrome have prelingual or postlingual sensorineural hearing impairment in early childhood, slowly progressive dystonia or ataxia in the teens, slowly progressive decreased visual acuity from optic atrophy beginning at approximately age 20 years, and dementia beginning at approximately age 40 years. Psychiatric symptoms such as personality change and paranoia may appear in childhood and progress. The hearing impairment appears to be consistent in age of onset and progression, whereas the neurologic, visual, and neuropsychiatric signs vary in degree of severity and rate of progression. Females may have mild hearing impairment and focal dystonia.
Autosomal dominant nonsyndromic hearing loss 9
MedGen UID:
371327
Concept ID:
C1832425
Disease or Syndrome
DFNA9 is an autosomal dominant adult-onset form of progressive sensorineural hearing loss associated with variable vestibular dysfunction (summary by Robertson et al., 2006).

Professional guidelines

PubMed

Nisenbaum E, Yan D, Shearer AE, de Joya E, Thielhelm T, Russell N, Staecker H, Chen Z, Holt JR, Liu X
Audiol Neurootol 2023;28(6):407-419. Epub 2023 Jun 16 doi: 10.1159/000528766. PMID: 37331337Free PMC Article
Galbis-Martínez L, Blanco-Kelly F, García-García G, Ávila-Fernández A, Jaijo T, Fuster-García C, Perea-Romero I, Zurita-Muñoz O, Jimenez-Rolando B, Carreño E, García-Sandoval B, Millán JM, Ayuso C
Acta Ophthalmol 2021 Dec;99(8):922-930. Epub 2021 Feb 11 doi: 10.1111/aos.14795. PMID: 33576163Free PMC Article
de Brouwer AP, van Bokhoven H, Nabuurs SB, Arts WF, Christodoulou J, Duley J
Am J Hum Genet 2010 Apr 9;86(4):506-18. doi: 10.1016/j.ajhg.2010.02.024. PMID: 20380929Free PMC Article

Recent clinical studies

Etiology

Pollak A, Mueller-Malesinska M, Lechowicz U, Skorka A, Korniszewski L, Sobczyk-Kopciol A, Waskiewicz A, Broda G, Iwanicka-Pronicka K, Oldak M, Skarzynski H, Płoski R
DNA Cell Biol 2012 Jul;31(7):1267-73. Epub 2012 Mar 16 doi: 10.1089/dna.2012.1607. PMID: 22424391Free PMC Article
Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH
Am J Otol 2000 Sep;21(5):675-81. PMID: 10993457

Diagnosis

Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH
Am J Otol 2000 Sep;21(5):675-81. PMID: 10993457

Clinical prediction guides

Aguirre LA, Pérez-Bas M, Villamar M, López-Ariztegui MA, Moreno-Pelayo MA, Moreno F, del Castillo I
Neuromuscul Disord 2008 Dec;18(12):979-81. Epub 2008 Oct 25 doi: 10.1016/j.nmd.2008.09.009. PMID: 18952432

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