A MOLECULAR PANORAMA OF DOWN SYNDROME- À LA MODE EVIDENCE AND FUTURE IMPLICATION
*Pramod Singh Khatri and Dr. Sumit Kumar
ABSTRACT
Down syndrome brought on by chromosome 21 (trisomy) is
the most well-known genetic reason of mental hindrance in
human population. Interruption of the phenotype is assumed
to be the aftereffect of gene dose unevenness. Therefore, the
majority of the chromosome 21 transcripts are attuned for the
gene dose impact. Overexpressed gene are most likely to be
responsible for the Down syndrome phenotype. Profoundly
variable genes could represent phenotypic varieties found in
such patients. Down syndrome influences many infants
worldwide independent of race, ethnicity, and maternal age at
gestation. Much investigation has been done to focus
precisely how the additional chromosome 21 leads severe fatal symptoms.
Keywords: Down Syndrome, HSA21, MTHFR, DYRK1A, Folate Metabolism.
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