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Wolfram-like syndrome
rareWolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings.
- Identifiers
- MONDO:0013673 OMIM:614296Orphanet:411590
- Causal genes
- WFS1
- Also known as
- WFSL · Wolfram-like syndrome, autosomal dominant
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