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Basic and Clinical Neuroscience، جلد ۱۳، شماره ۶، صفحات ۰-۰
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Repetitive suicidal behaviors in a case with a new mutation of Wolfram syndrome; A jump from the gene to the behavior |
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| چکیده انگلیسی مقاله |
Wolfram syndrome (WS) is a rare autosomal recessive neurodegenerative disease with variable symptoms, including neuropsychiatric manifestations. A 26-year-old man was reported with classic symptoms of WS and repetitive psychiatric hospitalizations and at least 16 suicidal attempts. The genetic study demonstrated a novel homozygous stop-codon mutation on the WFS1 gene. This special type of mutation may be related to repetitive suicidal behaviors in this case of WS. Psychological support should be a routine practice in patients with WS. |
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| کلیدواژه‌های انگلیسی مقاله |
Wolfram syndrome, suicidal behavior, gene mutation, WFS1 gene |
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| نویسندگان مقاله |
| Fatemeh Sadat Mirfazeli
Mental Health Research Center, Psychosocial Health Research Institute, Iran University of Medical Sciences, Tehran, Iran.
| Fatemeh Mohebi
School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
| Amin Jahanbakhshi
Skull Base Research Center, Neurosurgery Department, Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
| Omid Aryani
Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
| Mostafa Almasi-Dooghaee
Neurology Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
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| نشانی اینترنتی |
http://bcn.iums.ac.ir/browse.php?a_code=A-10-910-3&slc_lang=en&sid=1 |
| فایل مقاله |
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| کد مقاله (doi) |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
Clinical Neuroscience |
| نوع مقاله منتشر شده |
Original |
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