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MLS (Medical Laboratory Scientist) ASCP Exam 2026/2027 Newest exam with Verified Questions And 100% Corret Detailed Answers||Already Graded A+

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MLS (Medical Laboratory Scientist) ASCP Exam 2026/2027 Newest exam with Verified Questions And 100% Corret Detailed Answers||Already Graded A+

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MLS ASCP
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MLS ASCP

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December 6, 2025
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2025/2026
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MLS (Medical Laboratory Scientist) ASCP Exam

2026/2027 Newest exam with Verified Questions And

100% Corret Detailed Answers||Already Graded A+

The incidence fo hemolytic disease of the fetus and

newborn due to anti-D would be expected to be rarest in

which population? - ANSWER-Asians




Erythroleukemia: - ANSWER-Also known as Acute

Myelogenous Leukemia type M6. This type is associated

with either the presence of both erythroid and myeloid

precursors OR strictly erythroid precursors.

,2|Page


Myelomonocytic leukemia - ANSWER-Is associated with

an increase in myeloid and monocytic cell precursors, but

not red blood cell precursors




Species that are Lysine (+), arginine (=) and ornithine (+):

- ANSWER-Enterobacter aerogenes, Edwardsiella species

and most Serratia species




Lysine reaction for all Citrobacter: - ANSWER-Negative




Key identifying characteristic for Pantoa (Enterobacter)

agglomerans: - ANSWER-negative reactions for the three

decarboxylases commonly tested ( Lysine, arginine and

ornithine)

,3|Page




Which organism is MOST likely responsible for septic

reactions associated with Red Blood Cell transfusions? -

ANSWER-Yersina entercolitica is most likely responsible

for septic reactions in transfusions of Red Blood Cells.

This organism is usually acquired by ingestion of

contaminated food and causes mild symptoms of

abdominal pain and diarrhea. Growth of Y. entercolitica is

enhanced in iron-rich environments such as red cell

components.




Gaucher's disease - ANSWER-The most common

lysosomal storage disease caused by insufficient activity

of the lysosomal enzyme glucocerebrosidase that leads to

, 4|Page


the deposition of glucocerebroside in cells of the

macrophage-monocyte system.




Diseases associated with dysfunctions of

polymorphonuclear neutrophils (PMNs) - ANSWER-

Chediak-Higashi syndrome (CH), Chronic granulomatous

disease (CGD), Myeloperoxidase deficiency (MPO)




Nephrotic Syndrome: - ANSWER-Caused by damage to

the kidneys, especially the basement membrane of the

glomerulus; which causes abnormal excretion of protein

and red blood cells in the urine. Fats are also present in

the urine in most cases. A foamy appearance of the urine

is a key characteristic of this condition.
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