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sickle cell disease
How is Sickle Cell Disease Diagnosed?
SCD is commonly diagnosed through newborn screening, which involves a blood test that can detect the presence of HbS. If the screening test indicates SCD, confirmatory tests like hemoglobin electrophoresis or DNA analysis are performed.
Frequently asked queries:
What is Sickle Cell Disease?
How is Sickle Cell Disease Inherited?
How is Sickle Cell Disease Diagnosed?
What Types of Corrective Lenses Are Available?
Can Tight Uterine Contractions Be Prevented?
What Are the Challenges in Using Imaging Techniques?
What are Auditory Brainstem Responses (ABRs)?
How Can SIADH be Prevented in Pediatrics?
What is Limited Research in Pediatrics?
What Types of Grammar Errors Can These Tools Detect?
What is the Impact of Parental Role Modeling on Social Skills?
How is Brain Health Assessed in Pediatrics?
What Components are Included in a Comprehensive Program?
Why is the LES Immature in Newborns?
What Causes Developmental Disorders in Neonates?
How do Toxins Affect Children Differently?
What Preventive Measures are Available?
How Can Pediatricians Address Health Disparities in the Community?
How Can Nutrition Influence Tissue Health in Children?
What is Peripheral Neuropathy?
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