Sag pathophysiology signs pediatrics clinical endocrinology muscular workup dementia genetics

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2 results

Major neurocognitive disorders (MNCD): Diagnosis and workup

1) Clinical diagnosis Cognitive impairment + loss of autonomy
2)

1) Clinical ... (parkinsonian signs ... hyperorality, - 25% genetic ... Frontal atrophy Vascular ... #Diagnosis #Geriatrics

21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

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