ATI RN
Endocrine System Pediatric Questions
Question 1 of 5
Subjects with type 1 DM have evidence for celiac disease in
Correct Answer: A
Rationale: 5-10% (A) of type 1 DM patients have celiac disease, per screening studies.
Question 2 of 5
Signs of insulin resistance or conditions associated with insulin resistance in T2 DM in children include the following EXCEPT
Correct Answer: D
Rationale: PCOS (E) is associated but not a direct sign of insulin resistance; others (A-D) are.
Question 3 of 5
Inborn errors of metabolism (IEM) are hereditary biochemical disorders caused by single-gene mutations that result in alteration of
Correct Answer: D
Rationale: IEMs result from single-gene mutations altering enzyme function, typically affecting protein structure or production (e.g., enzymes), not chromosomes (A), mitochondria broadly (B), fats (C), or carbohydrates (E) as primary defects.
Question 4 of 5
A 6-year-old boy with eczematoid rash, abnormal face, and prominent maxilla complains from deterioration in school performance, hyperactivity, and seizures for the last 2 years. Of the following, the MOST likely enzymatic deficiency is
Correct Answer: D
Rationale: Phenylalanine hydroxylase deficiency (PKU) causes mental decline, seizures, rash, and facial changes from phenylalanine buildup, unlike lysosomal deficiencies (A, B, C) or tyrosinemia (E).
Question 5 of 5
A 15-month-old boy had recurrent hospital admissions because of fever, jaundice, subcutaneous bleeding, and hypoglycemic fits; on examination, there is hepatomegaly. In the last attack, the child developed severe legs pain associated with retraction of the neck and trunk. Of the following, the MOST likely diagnosis is
Correct Answer: D
Rationale: Tyrosinemia type 1 fits with recurrent fever, jaundice, bleeding, hypoglycemia, hepatomegaly, and neurological symptoms (pain, retraction) from tyrosine accumulation, unlike other conditions (A, B, C, E).