23 results
management differential disease neurology addisons adrenal insufficiency msk pulmonary secondary syndrome treatment urology workup 21hydroxylasedeficiency 21ohd adhesivecapsulitis als alzheimersdisease amyotrophic
Primary hypoadrenalism (Addison’s disease) – symptoms, signs #Diagnosis #Hypoadrenalism #Addisons #Disease #Hypoadrenalism #Signs #Symptoms ** GrepMed Recommended Text:
Primary hypoadrenalism ... , signs #Diagnosis ... #Symptoms ** ... GrepMed Recommended Text ... Basic and Clinical Endocrinology
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
Tuberculosis: can cause ... Serum DHEAS Diagnosis ... clue • Blood tests ... addisons #disease #endocrinology ... #diagnosis #signs
Hyperparathyroidism - Primary vs Secondary vs Tertiary Lab Comparison: • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
: Commonly no signs ... pain Psychiatric Symptoms ... Hyperparathyroidism #diagnosis ... #endocrinology ... #Tertiary #pathophysiology
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Adrenal Insufficiency - Diagnosis and Management Summary Primary Adrenal Insufficiency: Most Common Cause in the US: Autoimmune Adrenalitis Other
Management Summary Primary ... ketoconazole, etomidate) Symptoms ... A STIM test can ... ACTH STIM TEST: ... #Management #Endocrinology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
• Other rare causes ... Overproduction #diagnosis ... #signs #symptoms ... #endocrinology ... #pathophysiology
Cauda Equina Syndrome Causes: • Large lumbar degenerative disc herniation (central) • Severe lumbar spondylosis • Neoplasm
Equina Syndrome Causes ... reflexes) • Urinary ... Syndrome #MSK #pathophysiology ... #diagnosis #symptoms ... #signs
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 ... #genetics #endocrinology ... #peds #pediatrics
Uncommon Causes of Noncardiogenic Pulmonary Edema (NCPE) - Differential Diagnosis Framework High Altitude Pulmonary Edema: • Accumulation
- Differential Diagnosis ... - Dyspnea at rest ... • Signs/Symptoms ... • Signs/Symptoms ... #differential #diagnosis
Primary Biliary Cirrhosis (PBC) - Summary PBC Epidemiology: • Female:Male 9:1 • Common European descent • Age:
Primary Biliary ... 65 years PBC Pathophysiology ... intralobular bile ducts causes ... failure PBC Signs ... and Symptoms:
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