3 results
pediatrics 21hydroxylasedeficiency diagnosis genetics hypothyroid infant pathophysiology shock
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 ... #Peds #Pediatrics
Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
, Dry coarse skin ... #Hypothyroid #Features ... #Signs #Symptoms ... #Diagnosis #PhysicalExam ... #Endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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