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Loss of renal phosphate wasting in a child with autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation.
Horm. Res. Paediatr. 55, 305-308 (2001)
A girl with autosomal dominant hypophosphatemic rickets, presented with clinical, radiological and laboratory signs of rickets at the age of 11 months. She showed a good response to the treatment with low doses of oral phosphate and calcitriol. Surprisingly, she lost her renal phosphate wasting at the age of 8 years, indicating that the disturbed phosphate metabolism can be compensated by hormonal or other factors.
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Publication type
Article: Journal article
Document type
Scientific Article
Language
english
Publication Year
2001
HGF-reported in Year
0
ISSN (print) / ISBN
1663-2818
e-ISSN
1663-2826
Journal
Hormone Research in Paediatrics
Quellenangaben
Volume: 55,
Issue: 6,
Pages: 305-308
Publisher
Karger
Reviewing status
Peer reviewed
Institute(s)
Institute of Human Genetics (IHG)
PubMed ID
11805436
Erfassungsdatum
2001-12-31