11 results
diagnosis parathyroid symptoms calcitonin genetics hormone pediatrics secondary 21hydroxylasedeficiency 21ohd bulimianervosa calcitriol causes complications differential excess gh growthhormone homeostasis hyperparathyroidism
Hormonal Regulation of the Blood Calcium concentration #Calcium #Regulation #Parathyroid #Calcitonin #Calcitriol #PTH #Endocrinology #Pathophysiology #Hormones
Hormonal Regulation ... Calcitonin #Calcitriol #PTH ... #Endocrinology ... #Pathophysiology ... #Hormones
Effects of Parathyroid hormone (PTH) and Calcitonin on Calcium and Phosphate Metabolism #Parathyroid #hormone #PTH #Calcitonin #phosphate
of Parathyroid hormone ... (PTH) and Calcitonin ... on Calcium and ... phosphate #metabolism #pathophysiology ... #endocrinology
Parathyroid Hormone (PTH) Effect in Calcium and Phosphorus Calcium - Net Effect Hypercalcemia: ↑ intestinal
Parathyroid Hormone ... (PTH) Effect in ... #PTH #parathormone ... #pathophysiology ... #endocrinology
Hyperparathyroidism - Primary vs Secondary vs Tertiary Lab Comparison: • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
, ↑Calcium, ↑Vitamin ... , ↓→Calcium, ↓Vitamin ... Symptoms: Commonly no signs ... Hyperparathyroidism #diagnosis #endocrinology ... Secondary #Tertiary #pathophysiology
Calcium homeostasis is a process controlled by chiefly by hormones vitamin D and PTH. Vitamin D
by chiefly by hormones ... vitamin D and PTH ... #Pathophysiology ... #Endocrinology ... #PTH #VitaminD
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... delayed puberty -> Infertility ... #genetics #pathophysiology ... #peds #pediatrics
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
Growth Hormone Excess ... Carpal Tunnel Syndrome ... Overproduction #diagnosis #signs ... #symptoms #endocrinology ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
• Boerhaave syndrome ... Calcium, VitD) and ... lowered hormone ... Complications #pathophysiology ... #diagnosis #signs
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
hypertension and signs ... renal bruit or signs ... of hormonal excess ... Vasculitis • Endocrinologic ... apnea: CPAP, most pts
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