HARTMANS PHLEBOTOMY FINAL
EXAM TEST 2025/2026 NEWEST EXAM||Q&A FOR
GUARANTEED PASS||ALREADY
GRADED A+||LATEST UPDATE
Three parts to the screening test - ANSWER-Heel stick /
Blood sample
Pulse oximetry
Hearing test
When is the test done - ANSWER-when the newborn is 24
to 48 hours old
Positive result - ANSWER-does not confirm the condition
but warrants more testing
,Who is screened? - ANSWER-Every baby is screened
unless the parent for religions or personal reasons opt not
to test
Fatty Acid Oxiation Disorders - ANSWER-Anything with
chain in it
Carnitine Uptake defect / Carnitine ransport Defect
Trifunctional Protein Deficiency
Amino Acid Disorders - ANSWER-PKU
MSD
, Endocrine Disorders - ANSWER-Primary Congenital
Hypothyroidism
Congenital Adrenal Hyperplasia
Hemoglobin Disorders - ANSWER-SS Disease
Sickle Cell Anemia
S Beta Thalassemia
Biotinidase Deficiency - ANSWER-inadequate levels of
biotindase, enzyme that recycles water soluble vitamin
needed to process fats, proteins, & CHO
EXAM TEST 2025/2026 NEWEST EXAM||Q&A FOR
GUARANTEED PASS||ALREADY
GRADED A+||LATEST UPDATE
Three parts to the screening test - ANSWER-Heel stick /
Blood sample
Pulse oximetry
Hearing test
When is the test done - ANSWER-when the newborn is 24
to 48 hours old
Positive result - ANSWER-does not confirm the condition
but warrants more testing
,Who is screened? - ANSWER-Every baby is screened
unless the parent for religions or personal reasons opt not
to test
Fatty Acid Oxiation Disorders - ANSWER-Anything with
chain in it
Carnitine Uptake defect / Carnitine ransport Defect
Trifunctional Protein Deficiency
Amino Acid Disorders - ANSWER-PKU
MSD
, Endocrine Disorders - ANSWER-Primary Congenital
Hypothyroidism
Congenital Adrenal Hyperplasia
Hemoglobin Disorders - ANSWER-SS Disease
Sickle Cell Anemia
S Beta Thalassemia
Biotinidase Deficiency - ANSWER-inadequate levels of
biotindase, enzyme that recycles water soluble vitamin
needed to process fats, proteins, & CHO
