Purpose: Wolfram syndrome is characterized by early onset diabetes mellitus, diabetes insipidus, deafness, and optic atrophy, but retinal degeneration has not been described as a major component of the phenotype. We present two cases with Wolfram syndrome and evidence of retinal degeneration. Materials and Methods: Observational case series. Patients underwent complete ocular examinations as well as retinal imaging and electroretinography. Results: Both patients had electroretinographic evidence of retinal dysfunction/degeneration in addition to optic atrophy with an otherwise normal-appearing retina. Conclusions: Some patients with Wolfram syndrome have a mild retinal degeneration that may be a manifestation of the neuronal involvement tha...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
Purpose: Wolfram syndrome is an early onset genetic disease (1/160,000) featuring diabetes mellitus ...
SUMMARY: Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabe...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
Objective: Early diagnosis of syndromic monogenic diabetes allows for proper management and can lead...
Introduction: Wolfram syndrome is an autosomal recessive neurodegenerative disorder. Diabetes mellit...
Purpose To report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabetes in...
AbstractPurposeTo report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabete...
Wolfram syndrome (WFS) is a rare autosomal recessive neurodegenerative disease whose diagnosis requi...
PurposeTo report a case of Wolfram syndrome characterized by early onset diabetes mellitus and progr...
Wolfram Syndrome (WS) is an ultra-rare, progressive neurodegenerative disease characterized by earl...
Wolfram syndrome (WFS) is a rare disease inherited as an autosomal dominant trait. Type I diabetes m...
mellitus and progressive optic atrophy. Case Report: A 20-year-old male patient with diabetes mellit...
Wolfram syndrome is the association of diabetes mellitus, optic atrophy, diabetes insipidus and sens...
Background: Wolfram syndrome (WFS, OMIM: #222300) is an ultrarare autosomal recessive disorder chara...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
Purpose: Wolfram syndrome is an early onset genetic disease (1/160,000) featuring diabetes mellitus ...
SUMMARY: Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabe...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
Objective: Early diagnosis of syndromic monogenic diabetes allows for proper management and can lead...
Introduction: Wolfram syndrome is an autosomal recessive neurodegenerative disorder. Diabetes mellit...
Purpose To report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabetes in...
AbstractPurposeTo report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabete...
Wolfram syndrome (WFS) is a rare autosomal recessive neurodegenerative disease whose diagnosis requi...
PurposeTo report a case of Wolfram syndrome characterized by early onset diabetes mellitus and progr...
Wolfram Syndrome (WS) is an ultra-rare, progressive neurodegenerative disease characterized by earl...
Wolfram syndrome (WFS) is a rare disease inherited as an autosomal dominant trait. Type I diabetes m...
mellitus and progressive optic atrophy. Case Report: A 20-year-old male patient with diabetes mellit...
Wolfram syndrome is the association of diabetes mellitus, optic atrophy, diabetes insipidus and sens...
Background: Wolfram syndrome (WFS, OMIM: #222300) is an ultrarare autosomal recessive disorder chara...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
Purpose: Wolfram syndrome is an early onset genetic disease (1/160,000) featuring diabetes mellitus ...
SUMMARY: Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabe...