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endocrinology pediatrics 21hydroxylasedeficiency 21ohd causes dehydration diagnosis genetics hyperthyroidism infant pathophysiology thyroid
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Pale or Mottled Skin ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds
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 ... vomiting • Late (shock ... cold & mottled skin ... endocrinology #peds
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperthyroidism Overview Clinical ... Thickening of skin ... causes #diagnosis #differential ... endocrinology #signs ... #symptoms #thyroid
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