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The following points highlight the three major abnormalities of parathyroid function. The abnormalities are: 1. Hypoparathyroidism 2. Hyperparathyroidism 3. Deficiency of 1, 25(OH)2-D3.

Parathyroid Function: Abnormality # 1. Hypoparathyroidism:

a. The symptoms of hypoparathyroidism are muscular weakness, tetany and irritabil­ity.

b. In case, hypothyroidism begins early in childhood, there may be stunting of growth, defective tooth development, and mental retardation.

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c. Serum calcium is low, serum phosphate is increased, urinary calcium is low, serum magnesium and hydroxyproline levels are decreased.

d. Calcium, parathyroid hormone, and vita­min D precursors are used in the treatment of hypoparathyroidism.

Parathyroid Function: Abnormality # 2. Hyperparathyroidism:

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a. Hyperparathyroidism occurs due to a tumor of the gland. The symptoms of hy­perparathyroidism are hypercalcemia, de­calcification of bones causing pain and deformities, renal stones.

b. Serum phosphorus is low, serum alkaline phosphatase activity is increased, and ex­cretion of calcium in urine is highly increased.

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c. Removal of-tumor brings about prompt relief and injection of calcitonin helps to reduce serum calcium level.

Parathyroid Function: Abnormality # 3. Deficiency of 1, 25(OH)2-D3:

It stimulates intestinal absorption of calcium and phosphate.

a. 1, 25(OH)2-D3 is the only hormone that can promote the translocation of calcium against the concentration gradient which exists across the intestinal cell membrane. If controls the extracellular fluid Ca2+ in spite of marked fluctuations of the calci­um content of food.

b. It maintains a proper concentration of cal­cium and phosphate for deposition on the collagen fibrils in bone.

c. In 1, 25(OH)2-D3 deficiency, new bone formation slows and bone re-modelling is also impaired.

d. It also enhances the actions of parathy­roid hormones (PTH) on renal calcium reabsorption.

1, 25(OH)2-D3 acts at the cellular level just like steroid hormones:

a. There is nuclear accumulation of this hor­mone in pancreatic islet cells; some brain cells; some cells in the pituitary, ovary, testis, placenta, uterus, mammary gland, and thymus.

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b. The 1, 25(OH)2 D, receptor is a member of the steroid receptor family. The receptor has a DNA-binding domain that appears to contain the zinc finger motif character­istic of other steroid receptors.

c. The binding of the 1,25(OH)2-D3 receptor to chromatin in the nucleus suggests that 1, 25 (OH)2-D3 stimulates gene tran­scription and the formation of specific mRNAs.

d. Type 1 vitamin D-dependent rickets is an inherited autosomal recessive trait char­acterized by a defect in the conversion of 25(OH)-D3 to 1,25(OH)2-D3.

e. The formation of 1,25(OH)2-D3 is reduced by the loss of substantial renal parenchyma and calcium absorption decreases. Par­athyroid hormone is increased due to hypocalcemia.