Familial Hypophosphatemic Rickets (Hypophosphatemic Rickets, X-Linked Dominant; Rickets, X-Linked Hypophosphatemic)

A hereditary disorder characterized by hypophosphatemia; rickets; osteomalacia; renal defects in phosphate reabsorption and vitamin d metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.


Images

Fibroblast growth factor 23

'2p39': Crystal structure of human FGF23

Fibroblast growth factor 23

Fibroblast growth factor 23

(the currently featured pic at MCB) for an example of a picture generated using PDB data. I wouldn't rush things though, or get too strident about immediate deletion. It is clear the images are replaceable. I suggest getting WP:MCB on board to help find all such images that were obtained from the PDB, to tag them as replaceable and make a list, and then generate replacements and replace them. Pushing for immediate deletion may alienate people prepared to do work on this. Carcharoth (talk) 00:36, 20 February 2008 (UTC)

Fibroblast growth factor 23

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Fibroblast growth factor 23

Diagnosis and therapies

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Symptoms and diagnosis

Symptoms:

    

Wikipedia

Genetic disorder - WikipediaDent's disease - Wikipedia

More information

Reported cases - Summary of cases reported on this diseaseWHO - World Health OrganizationPubMed - A service of the National Library of Medicine and National Institutes of HealthMEDLINE - Literature from the National Library of MedicineMeSH - Medical Subject HeadingsDeCS - Health Sciences Descriptors
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