causes
congenital absence (DiGeorge syndrome) destruction (surgery, radiotherapy and malignancy) AI (can have other AI associations e.g. vitiligo and hypomagnesaemia)
presentation
diagnosis
low calcium, low PTH and high serum phosphate
idiopathic antibodies
Chvostek’s sign
Trousseau’s sign
management
calcium supplements
vitamin D tablets (alphacalcidol and cholecalciferol)
cause of pseudohypoparathyroidism
genetic defect in Gs alpha subunit (gene GNAS1) leading to low calcium and normal/high PTH
there is abnormality in the PTH receptor leading to resistance
presentation of pseudohypoparathyroidism
McCune Albright obesity subcutaenous calcification learning disability BUZZWORD= brachydactyly 4th metacarpal
diagnosis of pseudohypoparathyroidism
low calcium
high PTH
high phosphate
pseudo- pseudohypoparathyroidism
albright’s hereditary osteodystrophy but no alteration in PTH