impaired phagolysosome formation. Pathophys: Microtubule polymerization disorder means the "tracks" to get around the cell are broken, as such transport of phagosomes is deficient.
Back
congenital toxoplasmosis
Front
triad includes hydrocephalus, intracranial calcifications, and chorioretinitis
Back
Lynch
Front
Hereditary nonpolyposis colorectal cancer (HNPCC) ______ syndrome is an autosomal dominant genetic condition that is associated with a high risk of colon cancer
Back
Urine Bence Jones crystals
Front
Back
IL-4 & IL-5
Front
prominent role in mast cell function &, thus, atopic disorders
Back
IL-12 & IL-24
Front
produced by activated T cells & prominent in psoriasis
Back
macrosomia
Front
birth weight > 8lb, 14oz
Back
IL-2
Front
T & B lymphocytes proliferate when stimulated by_________.
Back
Proliferative glomerulonephritis
Front
post-strep glomerulonephritis is proliferative glomerulonephritis caused by type III hypersensitivity
Back
Autosomal Ressesive
Front
In general, most enzyme deficiency conditions follow an __________ inheritance pattern.
Back
Section 2
(26 cards)
nephrotic
Front
______________ syndrome marked by generalized edema and glomerulopathy
Back
Porphyria cutanea tarda
Front
skin fragility and blistering rash in sun-exposed areas, non-blanching palpable purpura
Back
lochia
Front
the postpartum vaginal discharge that typically continues for 4-6 weeks after childbirth
Back
xerosis
Front
asteatotic dermatitis, "winter itch"
Back
Acute Promyelocytic Leukemia
Front
t(15,17) responds to retinoic acid therapy
Back
upper motor neuron lesion
Front
Weakness
Increased muscle tone
Hyperreflexia
Babinski's sign
Hoffmann's sign
Posturing
Back
sarcoid
Front
polygonal, eosinophilic cells in the lung or intestine that produce serotonin
Back
IL-5
Front
cytokine for eosinophil activation, recruitment, & prolonged survival
Back
Interferon gamma
Front
secreted by helper T cells and activates macrophages
Back
nephritic
Front
_____________ syndrome characterized by hematuria and red blood cell casts