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| Open Access | FACTORS CAUSING MICROCEPHALY, DIAGNOSIS AND PREVENTION. ICD-10: (Q02)
Fozilova Asalxon Ikromjon qizi,Yuldasheva Muxlisa Muhammadjon qizi , Kokand University Andijan Branch Faculty of Medicine, General Medicine Program,Lecturer, Department of Microbiology, Virology and ImmunologyAbstract
This paper presents an overview of the etiology, clinical features, diagnostic methods, treatment and rehabilitation options, as well as prevention strategies for microcephaly. Microcephaly is a congenital or acquired condition characterized by a significantly smaller brain size compared to age- and sex-related norms and is often associated with delayed cognitive and physical development. The study provides a comprehensive analysis of primary and secondary forms of microcephaly, their association with genetic and environmental factors, as well as risk factors during pregnancy. The importance of prenatal and postnatal examinations in diagnosis is highlighted, along with the role of modern instrumental techniques such as computed tomography (CT) and magnetic resonance imaging (MRI). In addition, the significance of symptomatic treatment, rehabilitation measures, and preventive approaches is emphasized.
Keywords
Microcephaly, congenital anomalies, brain development, prenatal diagnosis, head circumference, genetic factors, Zika virus, neurological disorders, rehabilitation, epilepsy.
References
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Sadock B.J., Sadock V.A. Kaplan & Sadock’s Synopsis of Psychiatry. – Wolters Kluwer, 2019.
World Health Organization (WHO). Congenital anomalies and microcephaly: guidelines and reports.
Centers for Disease Control and Prevention (CDC). Microcephaly: Facts and Clinical Overview.
UpToDate. Evaluation and management of microcephaly in children.
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