Usher syndrome type 1J

Usher syndrome type 1J is a rare condition caused by a mutation in the CIB2 gene. It is one form of Usher syndrome, a group of disorders that can affect hearing and vision. This condition falls within the spectrum of genetic disorders where even small changes in the DNA can lead to significant effects on sensory functions. People with this condition may experience the impacts typical of Usher syndrome; however, detailed information about the specific presentation of type 1J is limited. Researchers have identified mutations in the CIB2 gene as the cause, and this finding is catalogued in references such as OMIM and GARD.

Information about symptoms is currently limited for this condition.

Usher syndrome type 1J is caused by a mutation in the CIB2 gene. This gene alteration leads to the development of the condition, and the genetic cause is well documented in medical databases such as OMIM.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.