Descriptor Portuguese: Hipofosfatemia Familiar. Synonyms English: Diabetes, Phosphate Familial Hypophosphatemia Hyperphosphaturia Phosphate Diabetes. [] Hipofosfatemia familiar Nefrocalcinose Nefrolitíase Osteomalácia Raquitismo Raquitismo hipofosfatêmico familiar Tomografia. Meanings of “hipofosfatemia” in English Spanish Dictionary: 1 result(s) Medicine. 1, Medicine, hipofosfatemia familiar · familial hypophosphatemia.

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Endocr Rev ;19 1: Isolation and structural identification of 1,dihydroxyvitamin D3 produced by cultured alveolar macrophages in sarcoidosis. Characterization of la hydroxylation of vitamin D3 sterols by cultured alveolar macrophages from patients with sarcoidosis. Serum levels of free 1,dihydroxyvitamin D in vitamin D toxicity. Current Opinion in Rheumatology Coexisting hyperparathyroidism with thyreotoxicosis.

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Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition disease. Familial articular chondrocalcinosis in Spain. J Bone Miner Res ;7 suppl 1: Stimulation by parathyroid hormone-related protein and transforming growth factor a of phosphate transport in osteoblast-like cells. Changes in markers of bone formation and resorption in a bed faniliar model of weightlessness.


N Eng J Med ; Parathyroid hormonerelated protein purified from a human lung cancer cell line. Similarity of synthetic peptide from human tumor to parathyroid in vivo and in vitro.

Services on Demand Journal. Hypercalcemia is a common underdiagnosed metabolic abnormality, since it is frequently asymptomatic.

Raquitismo e osteomalácia hipofosfatêmicos de origem genética mediados por FGF

Variable response to long-term 1 a-hydroxycholecalciferol in hemodialysis osteodistrophy. Familial articular chondrocalcinosis is a disorder characterized by deposition of calcium pyrophosphate dihydrate crystal in synovial fluid and articular cartilage that can cause joint pain and arthritis.

Familial articular hipofsofatemia in Quebec. Familial isolated primary hyperparathyroidism.

Cancer Res ; Multiple endocrine neoplasia type II. However, patients with hypercalcemia associated with malignancy are usually clinically very ill with mestatasis in multiple organs.

Parathyroid hormone-like peptide in normal and neoplastic fajiliar endocrine tissues.


Familial calcium pyrophosphate dihydrate deposition disease and the ANKH gene. Postgraduate Medicine ; 5: Therapy with colchicine was enough to prevent arthritic crisis in two patients and continous NSAID use was necessary to control symptoms in the last one. hipofosfatemai

Com a descoberta do PTHrP, este tem sido implicado na maioria destes casos. A clinically and genetically distinct syndrome.


Identification of a novel Inhibition by human interleukin-1 of parathyfoid hormone-related peptide effects on renal calcium and phosphorus metabolism in the rat.

Effect of transforming growth factor a and parathyroid hormone-related protein on phosphate transport in renal cells.

Hypercalcemia can less frequently be associated with some endocrine diseases like thyrotoxicosis, pheochromocytoma, Addison’s disease and multiple endocrine neoplasia types I and IIA. Basic and Clinical Concepts. Tumor necrosis factor enhances parathyroid hormone-related protein PTHrP -induced hypercalcemia and bone resorption without inhibiting bone formation in vivo.

hipofosfatemia familiar pdf

Secondary hypoadrenalism presenting with hypercalcaemia. J Biol Chem ; Pei Y, Herez Greenwood C, et al. Localisation of a gene for chondrocalcinosis to chromosome 5p. Parathyroid hormone-related peptide shares features with members of early response gene family: Condrocalcinose articular difusa CCAD.