AbstractPurposeTo report a case of Wolfram syndrome (WS) characterized by diabetes mellitus, diabetes insipidus, progressive optic atrophy, and deafness.Case reportA 19-year-old female patient, a known case of diabetes mellitus type I from six years before, presented with progressive vision loss since four years earlier. On fundoscopic examination, she had bilateral optic atrophy without diabetic retinopathy. The patient also had diabetes insipidus, neurosensory deafness, and neurogenic bladder.ConclusionWS should be considered a differential diagnosis in patients with diabetes mellitus who present with optic atrophy, and it is necessary to perform a hearing test as well as collecting 24-h urine output
Wolfram syndrome (WS) is typically an autosomal recessive disorder caused by biallelic variants in W...
Purpose: Wolfram syndrome is characterized by early onset diabetes mellitus, diabetes insipidus, dea...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
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 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...
PurposeTo report a case of Wolfram syndrome characterized by early onset diabetes mellitus and progr...
In 1938, Wolfram described a family in which four of eight siblings had diabetes mellitus and bilate...
Wolfram syndrome is the association of diabetes mellitus, optic atrophy, diabetes insipidus and sens...
Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease ...
atrophy and deafness). Three of the patients appear to have had very gradual onset of diabetes melli...
Introduction: Wolfram syndrome is an autosomal recessive neurodegenerative disorder. Diabetes mellit...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
A 15-year-old boy was referred because of bilateral hydroureteronephrosis. He had poorly controlled ...
Wolfram syndrome (WS) is typically an autosomal recessive disorder caused by biallelic variants in W...
Purpose: Wolfram syndrome is characterized by early onset diabetes mellitus, diabetes insipidus, dea...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...
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 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...
PurposeTo report a case of Wolfram syndrome characterized by early onset diabetes mellitus and progr...
In 1938, Wolfram described a family in which four of eight siblings had diabetes mellitus and bilate...
Wolfram syndrome is the association of diabetes mellitus, optic atrophy, diabetes insipidus and sens...
Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease ...
atrophy and deafness). Three of the patients appear to have had very gradual onset of diabetes melli...
Introduction: Wolfram syndrome is an autosomal recessive neurodegenerative disorder. Diabetes mellit...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
A 15-year-old boy was referred because of bilateral hydroureteronephrosis. He had poorly controlled ...
Wolfram syndrome (WS) is typically an autosomal recessive disorder caused by biallelic variants in W...
Purpose: Wolfram syndrome is characterized by early onset diabetes mellitus, diabetes insipidus, dea...
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed...