Which screening New born or Carrier or Diagnostic is used to identify a genetic condition in fast and efficient manner before life threatening symptoms arise,using chromosomal Micraroarray

Question

Which screening New born or Carrier or Diagnostic is used to identify a genetic condition in fast and efficient manner before life threatening symptoms arise,﻿using chromosomal Micraroarray

Accepted Answer

∻Answer∻ ⚹ Chromosomal Microarray (CMA) is used to identify genetic conditions in a fast and efficient manner before life-threatening symptoms arise. ⚹ ∻Solution∻ ‖ a ⋮ Chromosomal Microarray (CMA) ⋮ This is a powerful genetic test that can detect chromosomal imbalances, such as deletions or duplications, that are often not visible under a microscope. ‖ ‖ b ⋮ Newborn Screening ⋮ While newborn screening can detect certain genetic disorders, it is typically limited to a panel of specific conditions and may not identify all chromosomal abnormalities. ‖ ‖ c ⋮ Carrier Screening ⋮ This type of screening is used to identify individuals who carry a gene for a genetic disorder but may not show symptoms themselves. It is not typically used for diagnosing genetic conditions in newborns. ‖ ‖ d ⋮ Diagnostic Testing ⋮ Diagnostic tests such as CMA are used when a genetic condition is suspected in an individual, often based on physical symptoms or family history. ‖ ∻Key Concept∻ ⚹ Chromosomal Microarray (CMA) is the most comprehensive test for identifying genetic conditions before symptoms arise. ⚹ ∻Explanation∻ ⚹ CMA can detect a wide range of chromosomal imbalances, making it a fast and efficient diagnostic tool for genetic conditions in newborns. ⚹◊What specific genetic condition can be identified using chromosomal Microarray screening in newborns or carriers before life-threatening symptoms arise?⍭ Generate me a similar question◊

Sia