3 results
dementia diagnosis 21hydroxylasedeficiency alzheimersdisease classification differential endocrinology genetics mncd pediatrics peds signs subtypes symptoms workup
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... Complications: • Deficit ... AlzheimersDisease #Dementia ... #pathophysiology ... #geriatrics #diagnosis
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
functions - Aphaso-apraxo-agnosia ... atrophy Lewy body dementia ... (parkinsonian signs ... Frontotemporal dementia ... Workup #Diagnosis #Geriatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
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