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Congenital conductive hearing impairment

MedGen UID:
867179
Concept ID:
C4021537
Congenital Abnormality
Synonyms: Congenital conductive deafness; Congenital conductive hearing loss
SNOMED CT: Congenital conductive hearing loss (737344003)
 
HPO: HP:0008591

Definition

A type of conductive deafness with congenital onset. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVCongenital conductive hearing impairment

Conditions with this feature

Ossicular malformations, familial
MedGen UID:
371652
Concept ID:
C1833790
Disease or Syndrome
Thickened earlobes-conductive deafness syndrome
MedGen UID:
343676
Concept ID:
C1851896
Finding
Thickened earlobes-conductive deafness syndrome is characterized by microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant.

Professional guidelines

PubMed

Wei B, Zhou P, Zheng Y, Zhao Y, Li T, Zheng Y
Int J Pediatr Otorhinolaryngol 2023 Jan;164:111401. Epub 2022 Dec 8 doi: 10.1016/j.ijporl.2022.111401. PMID: 36512880
Karawani H, Matanis W, Na'ara S, Gordin A
Eur Arch Otorhinolaryngol 2023 Feb;280(2):643-649. Epub 2022 Jul 15 doi: 10.1007/s00405-022-07524-2. PMID: 35838783
Wrightson AS
Am Fam Physician 2007 May 1;75(9):1349-52. PMID: 17508530

Recent clinical studies

Etiology

Kunst SJ, Leijendeckers JM, Mylanus EA, Hol MK, Snik AF, Cremers CW
Otol Neurotol 2008 Jan;29(1):2-7. doi: 10.1097/mao.0b013e31815ee29a. PMID: 18199951

Diagnosis

Koch SM, Kumar S, Cremers CW
Arch Otolaryngol Head Neck Surg 2000 May;126(5):639-44. doi: 10.1001/archotol.126.5.639. PMID: 10807332

Clinical prediction guides

Siegbahn M, Jörgens D, Asp F, Hultcrantz M, Moreno R, Engmér Berglin C
Otol Neurotol 2024 Apr 1;45(4):e342-e350. Epub 2024 Feb 15 doi: 10.1097/MAO.0000000000004137. PMID: 38361347
Kunst SJ, Leijendeckers JM, Mylanus EA, Hol MK, Snik AF, Cremers CW
Otol Neurotol 2008 Jan;29(1):2-7. doi: 10.1097/mao.0b013e31815ee29a. PMID: 18199951

Supplemental Content

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