Renal rickets

Common Name(s)

Renal rickets

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Renal rickets" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Renal rickets" returned 10 free, full-text research articles on human participants. First 3 results:

A case of corneal cystinosis in a patient with rickets and chronic renal failure.
 

Author(s): Jae Yon Won, Hyung Bin Hwang, Sung Kun Chung

Journal: Indian J Ophthalmol. 2015 Oct;63(10):785-7.

 

A 22-year-old man diagnosed with nephropathic cystinosis at the age of 4 years was found to have progressive bilateral corneal crystal deposition. He presented with severe photophobia and decreased visual acuity. Ocular cystinosis was diagnosed on observing the typical crystals. Optical ...

Last Updated: 15 Dec 2015

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Relationship between rickets and incomplete distal renal tubular acidosis in children.
 

Author(s): Abiola O Oduwole, Olayiwola S Giwa, Rasheed A Arogundade

Journal:

 

In the Sub Saharan Africa Rickets has now been established to be due primarily to calcium deficiency and sometimes in combination with vitamin D deficiency. The main thrust of management is calcium supplementation with or without vitamin D. An observation was made that some children ...

Last Updated: 24 Aug 2010

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Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcifications.
 

Author(s): B Kremke, C Bergwitz, W Ahrens, S Schütt, M Schumacher, V Wagner, P-M Holterhus, H Jüppner, O Hiort

Journal: Exp. Clin. Endocrinol. Diabetes. 2009 Feb;117(2):49-56.

 

Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is caused by mutations in SLC34A3, the gene encoding the renal sodium-phosphate co-transporter NaPi-IIc. Despite increased urinary calcium excretion, HHRH is typically not associated with kidney stones prior to treatment. ...

Last Updated: 5 Feb 2009

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Renal rickets" returned 1 free, full-text review articles on human participants. First 3 results:

The journey from vitamin D-resistant rickets to the regulation of renal phosphate transport.
 

Author(s): Barton S Levine, Charles R Kleeman, Arnold J Felsenfeld

Journal: Clin J Am Soc Nephrol. 2009 Nov;4(11):1866-77.

 

In 1937, Fuller Albright first described two rare genetic disorders: Vitamin D resistant rickets and polyostotic fibrous dysplasia, now respectively known as X-linked hypophosphatemic rickets (XLH) and the McCune-Albright syndrome. Albright carefully characterized and meticulously ...

Last Updated: 7 Dec 2009

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Clinical Observation on Bone Metabolism Induced by Chronic Renal Insufficiency
 

Status: Recruiting

Condition Summary: Chronic Renal Insufficiency; Renal Osteodystrophy

 

Last Updated: 29 Nov 2016

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Iron Therapy for Autosomal Dominant Hypophosphatemic Rickets: A Pilot Project.
 

Status: Recruiting

Condition Summary: Autosomal Dominant Hypophosphatemic Rickets

 

Last Updated: 9 Aug 2017

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Renal Osteodystrophy: An Individual Management Approach
 

Status: Recruiting

Condition Summary: Kidney Failure, Chronic

 

Last Updated: 2 May 2017

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