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C19orf12 gene mutation with neuropsychiatric symptoms: a case report
被引:0
|作者:
Yildirim, Irem
[1
]
Altunc, Ali Tarik
[1
]
Gur, Ege
[2
]
Hacikurtes, Gamze
[2
]
Saglam, Nazife Gamze Usta
[1
]
Kiziltan, Gunes
[2
]
Turan, Senol
[1
]
机构:
[1] Istanbul Univ, Cerrahpasa Cerrahpasa Fac Med, Dept Psychiat, Istanbul, Turkiye
[2] Istanbul Univ, Cerrahpasa Cerrahpasa Fac Med, Dept Neurol, Istanbul, Turkiye
来源:
关键词:
C19orf12;
MPAN;
NBIA;
psychosis;
depression;
NEURODEGENERATION;
SUBTYPE;
D O I:
10.1080/13554794.2024.2426822
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Neurodegeneration with brain iron accumulation (NBIA) is a genetic disorder characterized by iron accumulation in the basal ganglia. Patients may develop behavioral abnormalities, dementia, movement disorders, and neuropsychiatric symptoms such as emotional lability, depression, anxiety, hallucinations, impulsivity, obsessions, and hyperactivity. In this case, a 46-year-old male patient with a C19orf12 mutation experienced depressive complaints before movement disorders, followed by cognitive deficits and psychotic symptoms as the disease progressed. The patient's response to quetiapine treatment is crucial for managing neuropsychiatric symptoms. This case could contribute to the literature on presentation, differential diagnosis, and management of neuropsychiatric symptoms in rare NBIA patients.
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页码:156 / 158
页数:3
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