Georgia Newborn Screening - Disorder Specific Info - 21022 update.pdf
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- Attached to
- Newborn Metabolic Screening (GA WACH)
- Solicitation number
- PANHCA25P0000008900
- Issued by
-
Department of the Army Medical Command
About this file
The document is a comprehensive newborn screening panel from the Georgia Department of Public Health, detailing disorders screened across four primary categories: Organic Acid Disorders, Fatty Acid Oxidation Disorders, Amino Acid Disorders, and Lysosomal Storage Disorders. The screening panel includes specific conditions within each category, such as Beta Ketothiolase, Carnitine Uptake Defect, Phenylketonuria, and Pompe Disease. Additional categories cover Endocrine Disorders, Hemoglobinopathy Disorders, Other Disorders, and Point of Care Screening Disorders, which include conditions like Congenital Adrenal Hyperplasia, Sickle Cell Anemia, Cystic Fibrosis, and Critical Congenital Heart Disease.
The document is associated with a Sources Sought Announcement for Newborn Metabolic Screening by Winn Army Community Hospital at Fort Stewart, Georgia. The market research seeks capabilities for metabolic screening tests aligned with the Recommended Uniform Screening Panel (RUSP) and the Official Code of Georgia. Interested parties are requested to provide contact information, capability statements matching Georgia Public Health testing requirements, and documentation demonstrating organizational capability to perform the specified newborn screenings. The announcement is for information gathering purposes and does not constitute a formal solicitation, with responses to be evaluated under NAICS code 621511 for Medical Laboratory Testing.
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Other files
| File | Type | Posted |
|---|---|---|
| GA Dept of Health NEWBORN PWS Redacted.pdf | ||
| rusp-july-2024.pdf |
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Source: https://www.babysfirsttest.org/newborn-screening
Georgia’s Newborn Screening Panel and Disorder Specific Information
Organic Acid Disorders • Beta Ketothiolase (BKT)
• Cobalamin A and B Deficiency (Cbl A,B )
• Glutaric Acidemia type I (GA1)
• 3-OH 3-CH Glutaric Aciduria (HMG)
• Isovaleric Acidemia (IVA)
• 3 Methylcrotonyl-Co A Carboxylase Deficiency (3MCC)
• Multiple Carboxylase Deficiency (MCD)
• Methylmalonic Acidemia (MMA)
• Propionic Acidemia
Fatty Acid Oxidation Disorders • Carnitine Uptake Defect
• Long Chain 3 hydroxyl acyl-CoA dehydrogenase
Deficiency (LCHADD)
• Medium Chain acyl-CoA dehydrogenase Deficiency
• Trifunctional Protein Deficiency (TFP)
• Very Long-chain acyl-CoA dehydrogenase
• Deficiency (VLCADD)
Amino Acid Disorders • Argininosuccinic Acidemia
• Citrullinemia
• Homocystinuria
• Maple Syrup Urine Disease (MSUD)
• Phenylketonuria (PKU)
• Tyrosinemia
Lysosomal Storage Disorders • Mucopolysaccharidosis I (MPSI)
• Pompe Disease https://www.babysfirsttest.org/newborn-screening http://www.babysfirsttest.org/newborn-screening/conditions/beta-ketothiolase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/beta-ketothiolase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/methylmalonic-acidemia-cobalamin-disorders http://www.babysfirsttest.org/newborn-screening/conditions/methylmalonic-acidemia-cobalamin-disorders http://www.babysfirsttest.org/newborn-screening/conditions/glutaric-acidemia-type-i http://www.babysfirsttest.org/newborn-screening/conditions/glutaric-acidemia-type-i http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/3-hydroxy-3-methylglutaric-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/isovaleric-acidemia http://www.babysfirsttest.org/newborn-screening/conditions/isovaleric-acidemia http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/3-methylcrotonyl-coa-carboxylase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/holocarboxylase-synthetase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/holocarboxylase-synthetase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/methylmalonic-acidemia-methymalonyl-coa-mutase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/methylmalonic-acidemia-methymalonyl-coa-mutase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/propionic-acidemia http://www.babysfirsttest.org/newborn-screening/conditions/propionic-acidemia http://www.babysfirsttest.org/newborn-screening/conditions/carnitine-uptake-defect http://www.babysfirsttest.org/newborn-screening/conditions/carnitine-uptake-defect http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/long-chain-l-3-hydroxyacyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/medium-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/trifunctional-protein-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/trifunctional-protein-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/very-long-chain-acyl-coa-dehydrogenase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/argininosuccinic-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/argininosuccinic-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/argininosuccinic-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/argininosuccinic-aciduria http://www.babysfirsttest.org/newborn-screening/conditions/homocystinuria http://www.babysfirsttest.org/newborn-screening/conditions/homocystinuria http://www.babysfirsttest.org/newborn-screening/conditions/maple-syrup-urine-disease-msud http://www.babysfirsttest.org/newborn-screening/conditions/maple-syrup-urine-disease-msud http://www.babysfirsttest.org/newborn-screening/conditions/classic-phenylketonuria-pku http://www.babysfirsttest.org/newborn-screening/conditions/classic-phenylketonuria-pku http://www.babysfirsttest.org/newborn-screening/conditions/tyrosinemia-type-i https://www.babysfirsttest.org/newborn-screening/conditions/mucopolysaccharidosis-type-i https://www.babysfirsttest.org/newborn-screening/conditions/pompe
Source: https://www.babysfirsttest.org/newborn-screening
Endocrine Disorders • Congenital Adrenal Hyperplasia (CAH)
• Congenital Hypothyroidism (CH)
Hemoglobinopathy Disorders • Sickle Cell Anemia
• Sickle Beta Thalassemia
• Sickle C Disease
• Other Hemoglobin Variants
Other Disorders
• Biotinidase Deficiency
• Cystic Fibrosis (CF)
• Galactosemia
• Krabbe Disease
• Severe Combined Immunodeficiency (SCID)
• Spinal Muscular Atrophy (SMA)
• X-linked Adrenoleukodystrophy (X-ALD)
Point of Care Screening Disorders • Critical Congenital Heart Disease (CCHD)
• Hearing Impairment
(rev 2/10/2022) https://www.babysfirsttest.org/newborn-screening http://www.babysfirsttest.org/newborn-screening/conditions/congenital-adrenal-hyperplasia http://www.babysfirsttest.org/newborn-screening/conditions/congenital-adrenal-hyperplasia http://www.babysfirsttest.org/newborn-screening/conditions/primary-congenital-hypothyroidism http://www.babysfirsttest.org/newborn-screening/conditions/primary-congenital-hypothyroidism http://www.babysfirsttest.org/newborn-screening/conditions/sickle-cell-anemia http://www.babysfirsttest.org/newborn-screening/conditions/sickle-cell-anemia http://www.babysfirsttest.org/newborn-screening/conditions/s-beta-thalassemia http://www.babysfirsttest.org/newborn-screening/conditions/s-beta-thalassemia http://www.babysfirsttest.org/newborn-screening/conditions/s-c-disease http://www.babysfirsttest.org/newborn-screening/conditions/s-c-disease http://www.babysfirsttest.org/newborn-screening/conditions/hemoglobinopathies http://www.babysfirsttest.org/newborn-screening/conditions/hemoglobinopathies http://www.babysfirsttest.org/newborn-screening/conditions/biotinidase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/biotinidase-deficiency http://www.babysfirsttest.org/newborn-screening/conditions/cystic-fibrosis-cf http://www.babysfirsttest.org/newborn-screening/conditions/cystic-fibrosis-cf http://www.babysfirsttest.org/newborn-screening/conditions/classic-galactosemia http://www.babysfirsttest.org/newborn-screening/conditions/classic-galactosemia https://www.babysfirsttest.org/newborn-screening/conditions/krabbe http://www.babysfirsttest.org/newborn-screening/conditions/severe-combined-immunodeficiency-scid https://www.babysfirsttest.org/newborn-screening/conditions/spinal-muscular-atrophy https://www.babysfirsttest.org/newborn-screening/conditions/adrenoleukodystrophy http://www.babysfirsttest.org/newborn-screening/conditions/critical-congenital-heart-disease-cchd http://www.babysfirsttest.org/newborn-screening/conditions/critical-congenital-heart-disease-cchd http://www.cdc.gov/ncbddd/hearingloss/index.html http://www.cdc.gov/ncbddd/hearingloss/index.html
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