Lecture 18 - Clinical Aspects of Hypocalcemia Flashcards
_______ syndrome arises from a 22q11.2 deletion. It results in absence of the _____ glands and dysplasia of the _____.
DiGeorge’s syndrome
Parathyroid glands
Thymus
Autoimmune polyglandular syndrome type 1 includes hypoparathyroidism, Addison’s disease, and mucocutaneous candidiasis. Look for young patients with low _____, low Ca++, and oral ______.
BP
Candidiasis
VitD deficiency can cause hypocalcemia. Specifically, VitD-dependent rickets type 1 arises from a deficiency in the _________ enzyme, whereas type two results from _________ receptor mutation.
1alpha-hydroxylase
1,25-vitD3 receptor
__________ is a class of medications associated with hypocalcemia.
Anticonvulsants (also Isoniazid!)
How do changes in QT interval compare with EKG of HYPER- vs HYPOcalcemic patient?
HYPER –> Shortened QT interval
HYPO –> prolonged QT
________ cataracts are one of the characteristic ocular symptoms of hypocalcemia.
Subcapsular
If given PTH, how will patients with Pseudohypocalcemia respond?
How should you treat them?
They won’t! They have PTH resistance.
Oral Ca++ supplementation with 1-2g elemental Ca++.
Remember that patients with chronic hypoparathyroidism should be supplemented with active _______.
VitD3
______ is a recombinant PTH drug injected subQ that has shown favorable outcomes in treatment of hypoparathyroidism.
______ diuretics can also be given to increase renal absorption of Ca++.
Natpara
Thiazide