3 results
diagnosis 21hydroxylasedeficiency endocarditis endocrinology generalized genetics grandmal infective marantic nbte neurology noninfective pediatrics pseudoseizures seizures symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
Generalized Seizures and Pseudoseizures Generalized seizures "are conceptualized as originating as some point within, and rapidly engaging,
general seizure caused ... and metabolic causes ... Pseudoseizures #GrandMal #Classification ... Diagnosis #Neurology #Signs ... #Symptoms #Comparison
Differentiating NBTE from Infective Endocarditis No pathognomonic signs/symptoms or echo features that are specific to NBTE, and
pathognomonic signs ... Frequent false-negative ... in up to 30% of cases ... #Endocarditis #comparison ... Marantic #diagnosis #table
No results found for "Negative comparison table causes classification signs pathophysiology classes peds 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Negative #comparison #table #causes #classification #signs #pathophysiology #classes #peds #21ohd