EXPLORING HIGH AUTISM RISK THROUGH COMMON GENETIC VARIANTS: A CLINICAL REPORT

Shamansurov Sh.Sh., Nurmatova Sh.O., Mirdjuraeva N.R.

Гуманитар ва табиий фанлар журнали · 2026-yil

Annotatsiya

Autism is a neurodevelopmental condition marked by difficulties in social interaction and communication, accompanied by restricted interests and repetitive behavioral patterns. It is widely prevalent, has a strong neurobiological basis, and demonstrates substantial heritability. The etiology of autism is multifactorial and heterogeneous, involving a wide range of genetic determinants, environmental exposures, and epigenetic regulatory mechanisms. Progress in molecular genetics, alongside large-scale epidemiological cohort studies, has enabled the identification of specific medical conditions, as well as genes and environmental contributors that are partially or fully implicated in its pathogenesis. These findings, correlated with clinical characteristics, help guide further research, refine clinical prognostic assessments, and support the development of more effective genetic counseling strategies.

Maqola ma’lumotlari
MualliflarShamansurov Sh.Sh., Nurmatova Sh.O., Mirdjuraeva N.R.
JurnalГуманитар ва табиий фанлар журнали
Nashr sanasi2026-02-01
Son30
TilRus

Kalit so‘zlar

autism spectrum disorder, exon, DNA, rehabilitation.

Ilmiy soha

Гуманитар ва табиий фанлар журнали jurnalidan boshqa maqolalar

Гуманитар ва табиий фанлар журнали — barcha maqolalar