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DEAFNESS, AUTOSOMAL RECESSIVE 2

Known as: DFNB2, NSRD2, Neurosensory Nonsyndromic Recessive Deafness 2 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal recessive inheritanceMYO7A geneVertigo

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran
Background: Hearing loss (HL) is the most frequent neurosensory impairment. HL is highly heterogeneous defect. This disorder… 
2017
2017
Bilateral Labyrinthine and Internal Auditory Canal Enhancement in an Infant With Severe Labyrinthine Dysplasia: A Previously Unreported Phenomenon.
OBJECTIVE To describe a novel case of congenital profound bilateral sensorineural hearing loss in a patient with bilateral… 
2013
2013
Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A
Variants in the head and tail domains of the MYO7A gene, encoding myosin VIIA, cause Usher syndrome type 1B (USH1B) and… 
2010
2010
Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families
Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non–syndromic. The aim of this… 
2002
2002
Searching for evidence of DFNB2.
Deafness is the most common form of sensory impairment in humans, affecting about 1 in 1,000 births in the United States. Of… 
2002
2002
The clinical presentation of DFNB2.
2001
2001
From DFNB2 to Usher syndrome: variable expressivity of the same disease.
1997
1997
Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.
Classical studies have demonstrated genetic heterogeneity for nonsyndromic autosomal recessive congenital neurosensory deafness… 
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