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| == Differential diagnosis == | | =Codes= |
| {| class="wikitable"
| | <div style="text-align: center;">'''Corrected total calcium = measured total calcium + 0.8 (4.0 − serum albumin)''' </div> |
| ! colspan="4" |Hypoparathyroidism
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| !Inheritance
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| !Gene mutation
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| !Clinical features
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| |Autoimmune
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| | ==References== |
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| | rowspan="6" |Isolated
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| |Familial Isolated hypoparathyroidism
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| | rowspan="2" |Autosomal dominant
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| |PTH gene
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| |[[GCM2]] gene
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| | rowspan="2" |Autosomal recessive
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| |PTH gene
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| |[[GCM2]] gene
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| |X-linked
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| |Autosomal dominant hypercalcemia
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| |Autosomal dominant hypocalcemia type 1
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| |Autosomal dominant hypocalcemia type 2
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| | rowspan="6" |Congenital multisystem syndromes
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| |'''[[DiGeorge syndrome]]'''
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| |'''[[CHARGE syndrome]]'''
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| |'''Kenny-Caffey syndrome type 1'''
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| |'''Kenny-Caffey syndrome type 2'''
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| |'''Sanjad-Sakati syndrome'''
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| |'''[[Barakat syndrome]]'''
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| | rowspan="6" |Metabolic diseases
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| | rowspan="2" |Mitochondiral polyneuropathies
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| |Kearns–Sayre syndrome
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| |Maternally inherited diabetes and deafness (MIDD)
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| | rowspan="2" |Mitochondrial enzyme deficiencies
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| |Mitochondrial trifunctional protein deficiency (MTP deficiency)
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| |Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (LCHAD deficiency)
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| | rowspan="2" |Heavy metal storage disorders
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| |Hemochromatosis
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| |Wilson's disease
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| |}
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| <references />
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| | | | | | | | | | | | | | | Hypercalcemia |
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| | | | | | | | Related to Parathyroid gland | | | | | | | | | | | | Unrelated to parathyroid gland | | |
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| | | Primary hyperparathyroidism | | | Secondary hyperparathyroidism | | | Tertiary hyperparathyroidism | | | | | | | | | |
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| Typical primary hyperparathyroidism | | Familial hypocalciuric hypercalcemia | | | | | | | | | | | | | | | | | | | |
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| | | | | | Malignancy | | | | | | Medication induced | | | | Nutritional | | | | | Granulomatous disease | | | Surgical | |
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| | | | Para-neoplastic syndrome: Parathyroid hormone related peptide | | Metaplasia: Hypercalcemia due to bone destruction | | Thiazide diuretics | | Lithium | | Milk alkali syndrome | | Vitamin D toxicity | | Sarcoidosis | | | Immobilization | |
Codes
Corrected total calcium = measured total calcium + 0.8 (4.0 − serum albumin)