Thrombotic Disorders — Flashcards

Hb _____ levels are increased in juvenile chronic myeloid leukemia (JMML)

_____ syndrome is the most common cause of megaloblastic anemia due to cobalamin deficiency in infancy in Western countries

The curative treatment for Chediak Higashi syndrome is _____

Acute chest syndrome is defined as a new _____ on CXR along with fever, respiratory distress, hypoxia, cough, or chest pain in a pt. with sickle cell disease

Kids with sickle cell disease should undergo _____ starting at age of 2 yrs to reduce the incidence of overt stroke

On serum analysis, patients with Systemic Juvenile Idiopathic Arthritis will frequently present with:- _____ RBCs- increased WBCs- increased TBCs

-thalassemia _____ is characterized by expansion of hematopoiesis into facial bones, leading to "chipmunk facies"

_____ syndrome is a syndrome of thrombocytopenia and consumptive coagulopathy in a patient of hemangioma

_____ is a common presenting sign of sickle cell anemia in infants (age group)