219 results
clinical ultrasound echocardiogram cardiology diagnosis a4c abdominal pulmonary lung effusion differential plax psax msk aortic gallbladder liver doppler neck renal
Secondary causes of Hypertension • Medications, Drugs, Chemo: NSAIDS, Steroids, CNI, Alcohol, Cocaine, OCP, Licorice, MAOI,
Secondary causes ... Other Endocrine causes ... low renin HTN causes ... Syndrome, 11B hydroxylase ... def, 17alpha hydroxylase
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hyperplasia - 21-Hydroxylase ... Reproductive: Gonadal hypofunction ... #Hyperplasia #Hydroxylase
Medications associated with neuroleptic malignant syndrome First-generation and second-generation antipsychotics are dopamine receptor antagonists, which produce a
of dopaminergic hypofunction ... Medications #Drugs #Causes
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
aldosterone Causes ... : Most Common Causes ... Tuberculosis: can cause ... Autoimmune: + 21-Hydroxylase ... ACTH - + 21-hydroxylase
Anosmia / Smell Dysfunction - Differential Diagnosis Algorithm Nasal Obstruction/ URTI: • Septal Deviation • Allergic Rhinitis
Mellitus • Adrenal Hypofunction ... • Adrenal Hyperfunction ... Diagnosis #Algorithm #Causes
Causes of Primary Amenorrhea - Differential Diagnosis Algorithm No onset of menarche by age 16 with secondary
Causes of Primary ... deficiency • 17- a Hydroxylase ... Mayer-Rokitansky-Küster-Hauser ... Diagnosis #Algorithm #Causes
Internal Jugular Vein Rouleaux Flow on POCUS Amazing video of a dilated IJV showing Rouleaux flow. Whenever
Rouleaux Flow on POCUS ... significantly, it causes ... echogenic as in this case ... for underlying cause ... Jugular #IJ #Vein #POCUS
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 Causes of Metabolic Alkalosis: Differential Diagnosis ECF volume contracted: urine chloride concentration <20 meq/L • Gastric alkalosis:
Causes of Metabolic ... hyperplasia: 11-ß hydroxylase ... deficiency, 17-a hydroxylase ... Differential #Diagnosis #Causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... enzyme 21-OHase causes
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
countries (11-24 cases ... Americans (18-71 cases ... mortality: 9-14 cases ... produce 1-alpha hydroxylase ... symptoms are not caused
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