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You are a evaluating a female patient at 5 day of life, who is brought by parents to
her first follow-up visit, referring exclusive breast feeding and jaundice 3 days of
evolution, cephalocaudal progression, no other associated symptoms. Parents
refer to be healthy, mother is 21 and father 25 years old. On examination she is
alert, responsive, with coarse facies, HR 156 bpm, RR 48 rpm, T. 36.8 C, with
jaundice in conjunctiva, trunk and upper extremities. 1.5cm posterior fontanelle,
cardiopulmonary without aggregates, abdominal umbilical hernia is reducible
approx. 3 cm in diameter, decreased muscle tone. You request laboratory tests,
confirming that the mother and the patient are blood group O positive, BT 19.2 mg /
dl, BI 15.6 mg / dl, metabolic screening with TSH 16.2.
A) Galactosemia
B) Congenital hypothyroidism
C) Blood group incompatibility
D) Biliary atresia
A) Cirrhosis
B) Kernicterus
C) Delayed psychomotor development
D) Heart Failure
3. What is the initial management of this patient?
A) Stop breastfeeding
B) Continuous phototherapy with eye protection
C) Start fasting and parenteral solutions
D) Exchange transfusin
A) Serum galactose
B) Scintigraphy liver and biliary tract
C) Complete thyroid profile
D) Direct Coombs
Case 2