Wolfram Syndrome
Wolfram Syndrome is an inherited disorder caused by a gene mutation that affects the endocrine system and the nervous system. It is a rare genetic disorder that is characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy, and deafness. Symptoms typically begin in childhood and vary from person to person. Wolfram Syndrome is a progressive, degenerative disorder, for which there is currently no known cure. Treatment focuses on managing symptoms, such as neurological and psychiatric problems, diabetes, and eye problems. Research has shown that early diagnosis and treatment of Wolfram Syndrome can help improve quality of life and prolong survival.
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