Calcium Disorder Flashcards
Two HYPERcalcemic Disorders with increase PTH
- Primary Hyper-parathyroidism
- Familial Hypo-CalciUric Hyper-Calcemia
Common clinical features of Primary Hyper-parathyroidism
Bones - Stones - Groans - Moans
- Bone pain
- Kidney stone
- Constipation/Abd pain
- Psychiatric
Disease Associated with Band Keratopathy
Primary Hyper-parathyroidism
Diagnosis for Primary HYPER-parathyroidism
- increase serum Ca++
- increase serum PTH
- decrease serum P
Calcimimetic Drug
Cinacalcet
Anti-Resorptive Bone Drug
- Bisphosphonate
- Denosumab
Causes of 2nd HYPER-Parathyroidism
Inducing PTH secretion:
- Increase Phosphorus
- Decrease Ca++
- Decrease 1,25 vit D
Hypercalcemia of Malignancy Lab
- Increase Ca++ & decrease P
- Decrease PTH
- Increase PTH-RP
Most common tumor type leading to Hypercalcemia of Malignancy
Lung Cancer (Squamous Cell)
Mechanism of Familial Hypocalciuric Hypercalcemia
Damage of Calcium Sensor Receptor
Lab for Familial Hypocalciuric Hypercalcemia
- Increase serum Ca++
- Increase serum PTH
- Decrease urine Ca++
- Decrease (urine Ca++/Creatinine clearance) < 0.1
HYPO-Calcemia Disorder with decrease PTH
- HYPO-Parathyroidism
How to correct Total serum Ca++ in HYPO-Proteinemia?
Add 0.8 mg/dl to total Calcium for every 1 g/L Albumin is < 4.0 g/L
ADD (4.0-serum albumin)* 0.8
Nutritional Vit D Deficiency Lab
- Decrease Serum Calcium
- Decrease Serum Phosphate
- Decrease Serum 25 (OH) Vitamin D
- Increase Serum PTH (2nd HPTH)
- Increase Serum Alkaline Phosphatase => suggests Osteomalacia
Vit D Disorders
- Acquired Vitamin D Deficiency
- Acquired 1,25 (OH)2 Vitamin D Deficiency
- Congenital 1 Alpha Hydroxylase Deficiency
=> “Vitamin D Dependent Rickets Type 1”
- Congenital Vitamin D Receptor Deficiency
=> “Vitamin D Dependent Rickets Type 2”