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Expanded Newborn screening + Congenital Hypothyroidism (CH)
SKU: MD-NLC826 Categories: , , , , , , , , , , Tags: , , , , , , ,

In Stock

Expanded Newborn screening + Congenital Hypothyroidism (CH)

฿13,600.00

Additional information

Also Known As

Newborn Screening Panel, NBS + CH, Comprehensive Newborn Screening + CH
Specimen

Dried blood spot on filter paper
Turnaround Time

18 Days
Test Code

MD-NLC826
Test Type

Special
Related Tests

PKU, Thyroid Function Tests

A comprehensive panel of tests performed on newborns to screen for various genetic, metabolic, and endocrine disorders, including congenital hypothyroidism. Early detection is crucial for preventing long-term health issues.

Product tags: Comprehensive Newborn Screening + CH, Developmental Delays, Genetic Disorders, Jaundice, Metabolic Disorders, NBS + CH, Newborn Screening Panel, None
Diseases: Genetic Disorders, Metabolic Disorders
Symptoms: Developmental Delays, Jaundice
Habits: None
Age Groups: Infants, Newborns
Specimens: Blood
Diagnostic Methods: Genetic Testing, Immunoassay
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Description

A comprehensive panel of tests performed on newborns to screen for various genetic, metabolic, and endocrine disorders, including congenital hypothyroidism. Early detection is crucial for preventing long-term health issues.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Newborn Screening Panel, NBS + CH, Comprehensive Newborn Screening + CH
Specimen

Dried blood spot on filter paper
Turnaround Time

18 Days
Test Code

MD-NLC826
Test Type

Special
Related Tests

PKU, Thyroid Function Tests

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