Autosomal recessive nonsyndromic hearing loss 28

An autosomal recessive disorder caused by mutations in the TRIOBP gene, encoding TRIO and F-actin-binding protein. The condition is characterized by severe to profound sensorineural hearing loss.

Also known as: autosomal recessive nonsyndromic hearing loss 28, DFNB28, TRIOBP autosomal recessive nonsyndromic deafness, autosomal recessive deafness 28, autosomal recessive nonsyndromic deafness 28, autosomal recessive nonsyndromic deafness caused by mutation in TRIOBP, autosomal recessive nonsyndromic deafness type 28, deafness, autosomal recessive 28

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 28 itself.