Maybe they were born with it
Where did the cells go
All things blood
100

What is one of the first symptoms infants and toddlers with SCD 

Sickle cell dactylics 

100

Whats the most likely diagnosis of a 4 y.o girl presents with:

2 weeks ago with viral infection, today acute onset bloody nose and petechial rash, hemoglobin normal, Platelets 4000, peripheral smear normal  expect lack of platelets 

ITP, immune thrombocytopenia 

100

What is the predominant hemoglobin at birth?

HbF

200

9 month old with 

Pallor, Irritability, poor growth, hepatosplenomegaly, jaundice 

What is the diagnosis ? 

Beta, thalassemia major aka Coolely anemia 

200

4 y.o old with follow labs 

low serum iron, high TIBC, low Transferrin, low ferritin

Whats the diagnosis 

Iron deficiency anemia 

200

What is the 1st site of RBC formation in the fetus ?

Yolk sac 


300

What is the leading cause of death in children and adults with SCD 

ACS - acute chest syndrome 

300

Whats the most likely diagnosis of a 4 y.o girl presents with:

Fever, oral ulcers, cervical lymphadenitis, occasional rectal and or vaginal ulcer and neutropenia. 

These signs and symptoms occur about every 21 day 

Cyclic neutropenia 

300

What organ produces most feta blood cells a 3 month?

Liver 

5-6 weeks liver takes over and peeks at 5 months 

400

What disease has these characteristics?

-point mutation at 6th codon of the bette globe gene located on the short arm of chromosome 11 

adenine is replace bu thymidine resulting in famine being encoded instead of glutamic acid 

Sickle cell disease 

400

9 y.o present with a hx of 

short stature, absent thumbs, abnormal radii. microcephaly, cafe au last spots, dark pigmentation, renal anomalies 

today presents with pallor, fatigue , bruising and petechiae. CBC show pancytopenia. 

Whats the diagnosis

Fanconi anemia 

400

What is the lifespan of a mature RBC 

120 days 

500

What congenital hereditary anemia has these characteristics?

- structural or functional abnormality of cytoskeleton protein, spectrum, ankyrin and less commonly bans 3 or protein 4.2 

-complications: cholelithiasis due to bilirubin stones and aplastic crisis form parvovirus infection 

Hereditary spherocytosis 

500

What syndrome has these findings: 

autosomal recessive, bleeding in the neonatal period, thrombocytopenia is severe nut rest of blood lines are normal, new for has no radii but normal thumbs. 

Thrombocytopenia-absent radius (TAR) syndrome 

500

which organ produces EPO in the fetus?

Liver