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Original publication





Book title


Publication Date



273 - 288


Hypoparathyroidism, Hypocalcemia, Hyperphosphataemia, DiGeorge syndrome, Autoimmune, Hypomagnesaemia, Pluriglandular disorder, Endocrinopathy, Normal serum calcium, Subcapsular cataract, Papilloedema, 25 Hydroxy vitamin D, 1,25 Dihydroxy vitamin D, Pseudohypoparathyroidism Tetany, Calcium gluconate, Celiac disease, Persistent hypocalcemia, Cholecalciferol, Ergocalciferol, Alfacalcidiol, Calcitriol, Hypercalciuria, Hypercalcemia, Autosomal disorder, X-linked disorder, Infiltrating metastases, Seizures, PTH gene mutation, Chromosome 11 p15, Autosomal dominant isolated hyperparathyroidism, Autosomal recessive hypoparathyroidism, Calcium receptor, GCMB gene, X-linked recessive hypoparathyroidism, Sox 3 gene, SRY gene, Acquired hypoparathyroidism, Hemochromatosis, Amyloidosis, Sarcoidosis, Thalassemia, Wilson's disease, Neonatal hypoparathyroidism, Kenney Caffey syndrome, Barakat syndrome, Dysmorphic features, Lymphoedema, Deafness, Renal dysplasia, Haploinsufficiency, Mitochondrial disorders, Kearns-Sayre syndrome, MELAS syndrome, Opthalmoplegia, Pigmentary retinopathy, Cardiomyopathy, Lactic acidosis, Diabetes mellitus, Sensorineural deafness, Trifunctional protein deficiency, Osteosclerosis, Nanophthalmos, Hyperopia, Kirk-Richardson syndrome, Sanjad-Sakati syndrome, Tubulin-specific chaperone, Brachytelephalangy, Blomstrand disease, Chondrodysplasia, Pluriglandular autoimmune hypoparathyroidism, Candidiasis, Hypogonadism, Steatorrhea, Alopecia, Vitiligo, Autoimmune polyglandular candidiasis ectodermal dystrophy, Polyglandular autoimmune type 1 syndrome, Autoantibodies, Addison's disease, Diabetes mellitus type 1, Inflammasome, Innate immune system, Familial benign hypocalciuric hypercalcemia, Barter syndrome type 5, Hypokalemic alkalosis, Hyperrenninemia, Hyperaldosteronism, Gain-of-function mutation, Inactivating mutation, Carpopedal spasm, Nephrocalcinosis, Autoimmune acquired hypoparathyroidism, Pseudohypoparathyroidism type 1a and 1b, Pseudopseudohypoparathyroidism, Albright's hereditary osteodystrophy, Dental hypoplasia, Brachydactyly, Adenyl cyclase, Parathyroid hormone-related protein, GNAS gene