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pathophysiology comparison differential management neurology adrenal classification complications criticalcare psychiatry sign syndrome 21hydroxylasedeficiency 21ohd addisons agammaglobulinemia anorexianervosa aortoenteric cah central
Syncope - Findings, Signs and Symptoms by Classification - Reflex Syncope - Cardiogenic Syncope
Syncope - Findings ... , Signs and Symptoms ... #Differential #Diagnosis ... Classification #Table ... #Symptoms #Findings
Shock - Findings, Signs and Symptoms by Classification - Hypovolemic (Intravascular volume depletion) - Distributive (Vasodilation)
Shock - Findings ... , Signs and Symptoms ... #Differential #Diagnosis ... Classification #Table ... #Symptoms #Findings
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... Pathophysiology #Signs ... #Symptoms #Diagnosis ... #Endocrinology
Characteristics of Peripheral and Central Vertigo PERIPHERAL VERTIGO • Onset: Sudden • Intensity: Severe initially, often decreasing
neuritis) • Neuro Findings ... None • Auditory Findings ... change • Neuro Findings ... #diagnosis #findings ... #signs #symptoms
Graves’ Disease: Pathogenesis and Clinical Findings B & T lymphocyte mediated autoimmunity attack TSH receptor -> Continuous
Pathogenesis and Clinical Findings ... the etiology Signs ... pathophysiology #endocin #endocrinology ... #symptoms #signs ... #diagnosis
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
21-Hydroxylase Deficiency ... - Signs and Symptoms ... #Hydroxylase #Deficiency ... #Signs #Symptoms ... #diagnosis #endocrinology
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
include protein C deficiency ... Aldosterone Deficiency ... Serum DHEAS Diagnosis ... addisons #disease #endocrinology ... #diagnosis #signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... Pathogenesis and Clinical Findings ... amount of enzyme deficiency ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
Pathogenesis and clinical findings ... Overproduction #diagnosis ... #signs #symptoms ... #endocrinology
Rapid, increasing signs of extrapyramidal symptoms (EPS) is an important key feature of NMS. EPS, associated
Rapid, increasing signs ... extrapyramidal symptoms ... Laboratory findings ... #Diagnosis #Serotonin ... NeurolepticMalignant #Comparison #Table
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