IntroductionEndocrinopathies and metabolic disorders-characterized thalassemic (T) patients and the prevention and treatment of these comorbidities are important targets to be achieved. The aim of the study was to analyze the diagnostic and prognostic role of ferritin for endocrinopathies and metabolic disorders in T patients. The ability of...
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2015 (v1)PublicationUploaded on: March 27, 2023
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2022 (v1)Publication
Wolfram syndrome 1, a rare autosomal recessive neurodegenerative disease, is caused by mutations in the WFS1 gene. It is characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD), and other clinical manifestations such as urological and neurological disorders. Here we described the case of a patient with an...
Uploaded on: April 14, 2023