[Wolfram-like syndrome: a case report].

Abstract excerpt

Different from classical autosomal recessive Wolfram syndrome, Wolfram-like syndrome is an autosomal dominant disorder caused by a heterozygous mutation in the WFS1 gene. In this case, a 7-year-old male child presented to the eye clinic due to vision loss that could not be corrected, discovered during a routine examination. The child had experienced hearing impairment since early childhood, leading to cochlear...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Child
• Share to Mutation
• Share to Optic Atrophy