ACCUPLACER READING
COMPREHENSION EXAM SCRIPT 2026
FULL SOLUTION QUESTIONS AND
ANSWERS GRADED A+
⩥ Trisomy 18.
Answer: Umbilical defect
Pyloric stenosis
Malrotation
TEF/EA
CHD
Abnormal Muscle tone
Microcephaly
Short sternum
Low-set malformed ears
Single umbilical artery
Rocker bottom feet
Growth deficiencies
Craniofacial defects
Acutis aplasia
Polydactyly
,Single Palmer crease
hand posturing with second and fifth digits overlapping third and fourth
⩥ Cri du chat syndrome.
Answer:
⩥ Cardiac anomalies associated with IDM babies.
Answer: VSD
TGV
PDA
Endocardial cushion defect
⩥ Noonan's Syndrome.
Answer: Second most common genetic syndrome
-webbing of neck
-Pectus excavatum
-cryptorchism
-pulmonary stenosis
⩥ Pompe Disease.
Answer: -Glycogen storage disease type II
-Autosomal recessive
, -marked cardiomyopathy
-Profound hypotonia and muscle weakness
- Hepatomegaly
-feeding difficulties
-respiratory distress
⩥ DIC Labs.
Answer: -Low platelets
-prolonged PT and PTT
-increased FSP
-decreased fibrinogen
-increased d-dimer which is the marker DIC
⩥ Albumin.
Answer: -Synthesized in the liver
-decreased in hepatocellular injury
⩥ Alk Phos.
Answer: -derived from liver, also found in bone, kidney, and small
intestine
-increased an obstructed bile disease, hepatitis, bone disease
COMPREHENSION EXAM SCRIPT 2026
FULL SOLUTION QUESTIONS AND
ANSWERS GRADED A+
⩥ Trisomy 18.
Answer: Umbilical defect
Pyloric stenosis
Malrotation
TEF/EA
CHD
Abnormal Muscle tone
Microcephaly
Short sternum
Low-set malformed ears
Single umbilical artery
Rocker bottom feet
Growth deficiencies
Craniofacial defects
Acutis aplasia
Polydactyly
,Single Palmer crease
hand posturing with second and fifth digits overlapping third and fourth
⩥ Cri du chat syndrome.
Answer:
⩥ Cardiac anomalies associated with IDM babies.
Answer: VSD
TGV
PDA
Endocardial cushion defect
⩥ Noonan's Syndrome.
Answer: Second most common genetic syndrome
-webbing of neck
-Pectus excavatum
-cryptorchism
-pulmonary stenosis
⩥ Pompe Disease.
Answer: -Glycogen storage disease type II
-Autosomal recessive
, -marked cardiomyopathy
-Profound hypotonia and muscle weakness
- Hepatomegaly
-feeding difficulties
-respiratory distress
⩥ DIC Labs.
Answer: -Low platelets
-prolonged PT and PTT
-increased FSP
-decreased fibrinogen
-increased d-dimer which is the marker DIC
⩥ Albumin.
Answer: -Synthesized in the liver
-decreased in hepatocellular injury
⩥ Alk Phos.
Answer: -derived from liver, also found in bone, kidney, and small
intestine
-increased an obstructed bile disease, hepatitis, bone disease
