Hypercalciuria: Difference between revisions
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Revision as of 16:19, 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, Thiazide diuretics |
Ear Nose Throat | No underlying causes |
Endocrine | Autosomal dominant hypoparathyroidism, Hypophosphatasia, Neonatal severe primary hyperparathyroidism, Cushing syndrome, Primary hyperparathyroidism, Hyperthyroidism, Pituitary tumour (growth hormone secreting) |
Environmental | 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
- Autosomal dominant hypoparathyroidism
- Bone metastases
- Cushing syndrome
- Dent disease
- Hyperparathyroidism, primary
- Hyperthyroidism
- Hypokalaemic distal renal tubular acidosis
- Hypophosphatasia
- Idiopathic hypercalciuria
- Immobility
- Metaphyseal chondrodysplasia, Jansen type
- Neonatal severe primary hyperparathyroidism
- Paget disease of bone
- Pituitary tumour (growth hormone secreting)
- Proximal renal tubular acidosis
- Sarcoidosis
- Vitamin D
- Wilson disease
- X-linked recessive nephrolithiasis type 1
- Zero gravity