Hypercalciuria: Difference between revisions
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Revision as of 16:50, 2 July 2012
Hypercalciuria | |
ICD-10 | E83.5 |
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ICD-9 | 791.9 |
DiseasesDB | 6220 |
MeSH | D053565 |
WikiDoc Resources for Hypercalciuria |
Articles |
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Most recent articles on Hypercalciuria Most cited articles on Hypercalciuria |
Media |
Powerpoint slides on Hypercalciuria |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Hypercalciuria at Clinical Trials.gov Trial results on Hypercalciuria Clinical Trials on Hypercalciuria at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Hypercalciuria NICE Guidance on Hypercalciuria
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Hypercalciuria Discussion groups on Hypercalciuria Patient Handouts on Hypercalciuria Directions to Hospitals Treating Hypercalciuria Risk calculators and risk factors for Hypercalciuria
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Healthcare Provider Resources |
Causes & Risk Factors for Hypercalciuria |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Lakshmi Gopalakrishnan, M.B.B.S. [2]
Overview
Hypercalciuria refers to elevated calcium in the urine. Chronic hypercalciuria may lead to impairment of renal function, nephrocalcinosis, and renal insufficiency.
Differential Diagnosis of Causes of Hypercalciuria
By Organ System
Cardiovascular | No underlying causes |
Chemical / poisoning | No underlying causes |
Dermatologic | No underlying causes |
Drug Side Effect | Vitamin D, Lithium, Calcitriol toxicity, Ethinyl estradiol and drospirnone, Furosemide, Glucocorticoids |
Ear Nose Throat | No underlying causes |
Endocrine | Cushing syndrome, Primary Hyperparathyroidism, Hyperthyroidism, Multiple endocrine neoplasia, Neonatal severe primary hyperparathyroidism, Parathyroid carcinoma, Pituitary tumour (growth hormone secreting), Primary parathyroid hyperplasia, Solitary parathyroid adenoma, Acromegaly |
Environmental | Dehydration, Immobility, Zero gravity |
Gastroenterologic | Wilson disease |
Genetic | Autosomal dominant hypoparathyroidism, Metaphyseal chondrodysplasia, Jansen type, Hypophosphatasia, Neonatal severe primary hyperparathyroidism, Wilson disease, X-linked recessive nephrolithiasis type 1 |
Hematologic | No underlying causes |
Iatrogenic | No underlying causes |
Infectious Disease | No underlying causes |
Musculoskeletal / Ortho | Metaphyseal chondrodysplasia, Jansen type |
Neurologic | No underlying causes |
Nutritional / Metabolic | No underlying causes |
Obstetric/Gynecologic | No underlying causes |
Oncologic | Bone metastases, Parathyroid tumor |
Opthalmologic | Wilson disease |
Overdose / Toxicity | No underlying causes |
Psychiatric | No underlying causes |
Pulmonary | No underlying causes |
Renal / Electrolyte | Dent disease, X-linked recessive nephrolithiasis type 1, Hypokalaemic distal renal tubular acidosis, Proximal renal tubular acidosis |
Rheum / Immune / Allergy | Sarcoidosis |
Sexual | No underlying causes |
Trauma | No underlying causes |
Urologic | No underlying causes |
Miscellaneous | Idiopathic hypercalciuria, Immobility, Paget disease of bone |
In alphabetical order
- Acute pyelonephritis
- Aminoaciduria
- Autosomal dominant hypocalcemia
- Autosomal dominant hypoparathyroidism
- Autosomal recessive Familial hypomagnesemia with Hypercalciuria and nephrocalcinosis
- Bartter syndrome
- Bone metastases
- Calcitriol toxicity
- Chronic hypokalemia
- Congenital hypothyroidism
- Cushing syndrome
- Cystinosis
- Dehydration
- Dent disease
- Ethinyl estradiol and drospirnone
- Excess Calcium intake
- Fanconi syndrome
- Fractures
- Furosemide
- Glucocorticoids
- Glycogen storage disease type 1a
- Hartnup disease
- Hereditary hypophosatemic rickets
- Histoplasmosis
- Hyperchloremic acidosis
- Hyperparathyroidism, primary
- Hyperthyroidism
- Hypocitraturia
- Hypokalaemic distal renal tubular acidosis
- Hypophosphatasia
- Idiopathic hypercalciuria
- Immobility
- Leukemia
- Lowe's syndrome
- Lymphoma
- McCune-Albright syndrome
- Medullary cystic kidney disease
- Medullary sponge kidney
- Metaphyseal chondrodysplasia, Jansen type
- Milk-alkali syndrome
- Multiple endocrine neoplasia
- Multiple myeloma
- Neonatal severe primary hyperparathyroidism
- Nephrocalcinosis
- Osteogenesis Imperfecta
- Osteoporosis
- Parathyroid carcinoma
- Paget disease of bone
- Pituitary tumour (growth hormone secreting)
- Primary parathyroid hyperplasia
- Proximal renal tubular acidosis
- Recumbency
- Reticulum cell sarcoma
- Sarcoidosis
- Solitary parathyroid adenoma
- Tuberculous granulomas
- Ulcerative colitis
- Vitamin D
- Williams syndrome
- Wilson disease
- X-linked recessive nephrolithiasis type 1
- Zero gravity
- Acromegaly