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diagnosis pathophysiology differential endocrinology genetics 21hydroxylasedeficiency 21ohd alzheimersdisease associated disorder disorders features geriatrics headache hypothyroid management mnemonic ms multiple neurocognitive
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
and signs. ... Symptoms: Tiredness ... intolerance, Poor memory ... slowness, Psychosis/dementia ... Carpal timel syndrome
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
mutations - Down syndrome ... chromosome 21) Signs ... semantic memory ... AlzheimersDisease #Dementia ... #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... , sleep apnea, cor ... pathophysiology #peds ... #pediatrics
HIV-Associated Neurocognitive Disorder (HAND) Definition: HIV-Associated Neurocognitive disorders categories: • Asymptomatic neurocognitive impairment • Mild neurocognitive impairment • HIV dementia Pathophysiology: HIV frequently
Disorder (HAND) ... dementia Pathophysiology ... • Depressive symptoms ... The clinical syndrome ... #AIDS #Neurology
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
and signs below ... , HIV, CMV, HTLV ... MCTD, Sjogren syndrome ... disorders #diagnosis #neurology ... differential #algorithm
Approach to Headaches - Differential Diagnosis Algorithm Red flags (PHANTOMS): • Pattern change, progressively worse, papilledema •
papilledema • Horner syndrome ... history of cancer, HIV ... ) • Systemic symptoms ... and signs (e.g. ... #neurology #PHANTOMS
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
• Or brainstem syndromes ... Signs and symptoms ... Progressive MS (Spinal cord ... objective evidence of neurologic ... • Acute: - IV
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Signs/Symptoms/Complications ... Late (shock): cold ... endocrinology #peds ... #pediatrics
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