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pediatrics 21hydroxylasedeficiency 21ohd dehydration endocrinology genetics pathophysiology symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant ... Pale or Mottled Skin ... #Signs #Symptoms ... #Shock #Infant
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
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