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differential geriatrics pathophysiology rheumatology scleroderma subtypes workup 21hydroxylasedeficiency 21ohd addisons alzheimersdisease cah calcium congenital cushings deficiency diffuse disease evaluation falls
The Dementia Umbrella Dementia is an umbrella term that describes a collection of symptoms that are caused
Dementia is ... collection of symptoms ... #Differential #Diagnosis ... Types #Subtypes #Classification ... #Geriatrics
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
and signs. ... Symptoms: Tiredness ... slowness, Psychosis/dementia ... #Symptoms #Diagnosis ... #PhysicalExam #Endocrinology
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
disorders (MNCD): Diagnosis ... 1) Clinical diagnosis ... (parkinsonian signs ... Differential #Subtypes #Classification ... #Geriatrics #Workup
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
vomiting • Fatigue Signs ... Reduced libido • Signs ... Serum DHEAS Diagnosis ... addisons #disease #endocrinology ... #diagnosis #signs
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... AlzheimersDisease #Dementia ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hydroxylase Deficiency - Signs ... and Symptoms • ... Hydroxylase #Deficiency #Signs ... #Symptoms #diagnosis ... #endocrinology
Symptoms and Signs of Hypocalcemia Muscular: Weakness, fatigue, Spasms, cramps Neurologic: Tetany, Chvostek sign, Trousseau sign, Circumoral and
Symptoms and Signs ... Hallucinations, dementia ... #Hypocalcemia #Symptoms ... #Signs #diagnosis ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Systemic Sclerosis (Scleroderma) Multi-system autoimmune disease characterized by vasculopathy and progressive fibrosis of skin and internal organs 3
thickening, distal to elbows ... skin thickening Signs ... and Symptoms: ... #rheumatology #diagnosis ... #signs #symptoms
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
pheochromocytomas are extra-adrenal ... bilateral, malignant, pediatric ... life • M=F Symptoms ... and Signs: 50% ... and signs: •
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