The area of the intestines where iron is absorbed
Duodenum
This is the most common cause of non-immune hemolytic anemia
Hereditary Spherocytosis
Tetramers of gamma globins
Hemoglobin Barts
Hereditary spherocytosis is typically a ____ mutation in spectrin or ankrin, less commonly protein 4.2 or band 3
Autosomal Dominant
Platelets are stored at this temperature
Room temperature or 24*C
Overconsumption of milk leads to iron deficiency by what mechanism (s)
Microvillus sloughing and depression of iron absorption
Helmet cells, bite cells, Heinz bodies and spherocytes are all signs of this hemolytic anemia
G6PD deficiency
--/alpha -
Hemoglobin H disease/Alpha Thalassemia intermedia
Hereditary pyropoikilocytosis is a ______ mutation in spectrin leading to severe anemia in childhood that improves in adulthood
Atosomal recessive
This is the only way to prevent TA-GVHD
Irradiation
The order of lab values to correct in iron deficiency anemia being treated with supplemental iron
Hemoglobin
RBC indicies (MVC MCHC)
Transferring & TIBC
Ferritin
Alloimmunization but not hemolysis does occur in the first pregnancy with this most immunogenic blood antigen
Rh
Mom B/B0
Dad B/B+
Odds child will have beta thalassemia intermedia
Odds child will have beta thalassemia trait
25%
50%
A 4 yo boy has a spider bite that gets infected and is placed on bactrim. 2 days later he is brought to the ER for severe abdominal pain, yellow color, fatigue and headache. How is this disorder inherited?
X-linked recessive
this evaluates compatibility between the donor blood and the recipient
Crossmatch
Drinking unpasturized goat's milk will lead to this deficiency
Folate
IgG mediated, Extravascular coombs positive hemolytic anemia
Warm Reactive Autoimmune Hemolytic Anemia
--/-- leads to severe transfusion dependent anemia requiring in-utero transfusions and HSCT for survival
Hydrop fetalis
Mom has alpha thalassemia trait cis mutation
Dad normal
odds children will have alpha thalassemia minor
50%
Name 2 plasma indications
DIC
Liver failure
Warfarin reversal
factor deficiency and no factor available
Plasma exchange
Vitamin B12 deficiency will lead to defective DNA synthesis causing megaloblastic anemia and what other side effects?
Jaundice
glossitis
Neurological deficits
Reticulocytopenia
Hypersegmented neutrophils
Seen in vasculitis, DIC, TTP, HUS, congenital heart disease
Schistocytes
This leads to free radicals and ROS species that damage organs leading to heart, liver and pituitary failure in patients with hemoglobinopathies
Iron overload or hemochromotosis
Mom alpha thalassemia minor trans mutation
Dad normal
Odds children will have alpha thalassemia trait vs normal vs silent carrier
100% silent carrier
4 hours after blood transfusion patient presents with fever, shortness of breath, pulmonary edema, hypotension
TRALI