Ad
related to: eclinpath hypophosphatemia- Adult Signs & Symptoms
Connect Their Symptoms
And Take The Right Next Steps.
- What Is XLH
Learn About The Causes, Impact
And Misdiagnosis Of XLH.
- How To Diagnose XLH
Find Helpful Info On Diagnosing
Pediatric & Adult XLH Patients.
- XLH Management
Learn About The Importance Of
Early Management Of XLH.
- Patient Case Studies
View Case Studies Of Pediatric
& Adult Patients With XLH.
- Video Library
Watch A MOD Video To Understand
How XLH Impacts Patients.
- Adult Signs & Symptoms
Search results
Results From The WOW.Com Content Network
Hypophosphatemia is an electrolyte disorder in which there is a low level of phosphate in the blood. [1] Symptoms may include weakness, trouble breathing, and loss of appetite. [ 1 ] Complications may include seizures , coma , rhabdomyolysis , or softening of the bones .
Blood tests reveal low levels of phosphate (hypophosphatemia) and inappropriately normal levels of vitamin D. [1] Occasionally, hypophosphatemia may improve over time as urine losses of phosphate partially correct. [1] ADHR may be lumped in with X-linked hypophosphatemia under general terms such as hypophosphatemic rickets.
Hypophosphatasia (/ ˌ h aɪ p oʊ ˈ f ɒ s f eɪ t ˌ eɪ ʒ ə /; also called deficiency of alkaline phosphatase, phosphoethanolaminuria, [5] or Rathbun's syndrome; [1] sometimes abbreviated HPP [6]) is a rare, and sometimes fatal, inherited [7] metabolic bone disease. [8]
X-linked hypophosphatemia (XLH) is an X-linked dominant form of rickets (or osteomalacia) that differs from most cases of dietary deficiency rickets in that vitamin D supplementation does not cure it. It can cause bone deformity including short stature and genu varum (bow-leggedness).
8074 64654 Ensembl ENSG00000118972 ENSMUSG00000000182 UniProt Q9GZV9 Q9EPC2 RefSeq (mRNA) NM_020638 NM_022657 RefSeq (protein) NP_065689 NP_073148 Location (UCSC) Chr 12: 4.37 – 4.38 Mb Chr 6: 127.05 – 127.06 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Fibroblast growth factor 23 (FGF-23) is a protein and member of the fibroblast growth factor (FGF) family which participates ...
Pages for logged out editors learn more. Contributions; Talk; Hypophosphataemia
Pages for logged out editors learn more. Contributions; Talk; Hypophosphatemia, familial
Oncogenic osteomalacia, also known as tumor-induced osteomalacia or oncogenic hypophosphatemic osteomalacia, is an uncommon disorder resulting in increased renal phosphate excretion, hypophosphatemia and osteomalacia. It may be caused by a phosphaturic mesenchymal tumor.
Ad
related to: eclinpath hypophosphatemia