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Syndromic genetic hearing loss

MedGen UID:
832341
•Concept ID:
CN206426
•
Disease or Syndrome
Synonym: Syndromic genetic deafness
 
Orphanet: ORPHA90642

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSyndromic genetic hearing loss
Follow this link to review classifications for Syndromic genetic hearing loss in Orphanet.

Professional guidelines

PubMed

Alport Syndrome: Achieving Early Diagnosis and Treatment.
Kashtan CE
Am J Kidney Dis 2021 Feb;77(2):272-279. Epub 2020 Jul 22 doi: 10.1053/j.ajkd.2020.03.026. PMID: 32712016
Wolfram Syndrome: Diagnosis, Management, and Treatment.
Urano F
Curr Diab Rep 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6. PMID: 26742931Free PMC Article
The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes.
Karaa A, Goldstein A
Pediatr Diabetes 2015 Feb;16(1):1-9. Epub 2014 Oct 20 doi: 10.1111/pedi.12223. PMID: 25330715

Recent clinical studies

Diagnosis

An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.
Ghasemnejad T, Shekari Khaniani M, Zarei F, Farbodnia M, Mansoori Derakhshan S
Int J Pediatr Otorhinolaryngol 2017 Jun;97:113-126. Epub 2017 Apr 6 doi: 10.1016/j.ijporl.2017.04.007. PMID: 28483220
The diagnosis of syndromic genetic hearing loss: a new proposal for an international cooperation.
Grisanti G, Grisanti S
Scand Audiol Suppl 1997;45:45-6. PMID: 9309826
Worldwide analysis and collection centre for data on syndromic genetic hearing loss: a new proposal.
Grisanti G
Scand Audiol Suppl 1996;42:23-5. PMID: 8668902

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
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    Consumer resources

    Reviews

    Related information

    • PMC Articles
      Related information in PubMed Central Links
    • PubMed
      Related literature resources in PubMed

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