The article presents clinical cases with a diagnosis of congenital and acquired microcephaly encountered in our work. We believe that it is necessary to conduct a study on this nosology based on a deep analysis of modern scientific data and literature. Among the regions of our republic, it is possible to determine the phenotypic and genotypic characteristics of microcephaly and study the molecular genetic aspects of congenital microcephaly, which will allow in the future to consult families affected by this disease in our region for the development of a medical genetics system. And this creates a basis for planning and improving activities for patients with these diseases.
| Mualliflar | Умида Тулкиновна Омонова, Мирзаолим Фозилжонович Холматов |
|---|---|
| Jurnal | Журнал неврологии и нейрохирургических исследований / Journal of Neurology and Neurosurgical Research |
| Nashr sanasi | 2025-04-08 |
| Jild | 6 |
| Son | 2 |
| Til | O‘zbek |
врожденная и приобретенная микроцефалия, клиническое течение, диагностика, метод полноэкзомного секвенирования, congenital and acquired microcephaly, clinical course, diagnostics, whole exome sequencing method, туғма ва орттирилган микроцефалиялар, клиник кечуви, ташхислаш, тўлиқ экзом секвенирлаш усули
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