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Sökning: id:"swepub:oai:DiVA.org:uu-392900" > Gaucher Disease in ...

Gaucher Disease in Bone : From Pathophysiology To Practice

Hughes, Derralynn (författare)
Royal Free London NHS Fdn Trust, London, England;UCL, London, England
Mikosch, Peter (författare)
Landesklinikum Mistelbach, Dept Internal Med 2, Mistelbach, Austria;Med Univ Vienna, Externe Lehre, Vienna, Austria
Belmatoug, Nadia (författare)
Univ Hosp Paris Nord Val de Seine, Assistance Publ Hop Paris, Dept Internal Med, Referral Ctr Lysosomal Dis, Clichy, France
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Carubbi, Francesca (författare)
Univ Modena & Reggio Emilia, NOCSAE Hosp, AOU Modena, Dept Biomed Metab & Neural Sci, Modena, Italy
Cox, Timothy M. (författare)
Univ Cambridge, Dept Med, Cambridge, England
Goker-Alpan, Ozlem (författare)
Lysosomal Disorders Res & Treatment Unit, Fairfax, VA USA
Kindmark, Andreas, 1967- (författare)
Uppsala universitet,Endokrinologi och mineralmetabolism
Mistry, PramodK (författare)
Yale Univ, Sch Med, Dept Internal Med Digest Dis, New Haven, CT USA
Poll, Ludger (författare)
Heinrich Heine Univ Dusseldorf, Practice Radiol & Nucl Med Duisburg Moers, Duisburg, Germany
Weinreb, Neal (författare)
Univ Miami, Miller Sch Med, Dept Human Genet, Coral Gables, FL 33124 USA;Univ Miami, Miller Sch Med, Dept Med Hematol, Coral Gables, FL 33124 USA
Deegan, Patrick (författare)
Addenbrookes Hosp, Lysosomal Disorders Unit, Box 135,Hills Rd, Cambridge CB2 0QQ, England
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 (creator_code:org_t)
2019-06-24
2019
Engelska.
Ingår i: Journal of Bone and Mineral Research. - : Wiley. - 0884-0431 .- 1523-4681. ; 34:6, s. 996-1013
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
Stäng  
  • Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunction in multiple organs. Involvement of the skeleton is one of the most prevalent aspects of GD and a major cause of pain, disability, and reduced quality of life. Uniform recommendations for contemporary evaluation and management are needed. To develop practical clinical recommendations, an international group of experienced physicians conducted a comprehensive review of 20 years' of the literature, defining terms according to pathophysiological understanding and pointing out best practice and unmet needs related to the skeletal features of this disorder. Abnormalities of bone modeling, reduced bone density, bone infarction, and plasma cell dyscrasias accompany the displacement of healthy adipocytes in adult marrow. Exposure to excess bioactive glycosphingolipids appears to affect hematopoiesis and the balance of osteoblast and osteoclast numbers and activity. Imbalance between bone formation and breakdown induces disordered trabecular and cortical bone modeling, cortical bone thinning, fragility fractures, and osteolytic lesions. Regular assessment of bone mineral density, marrow infiltration, the axial skeleton and searching for potential malignancy are recommended. MRI is valuable for monitoring skeletal involvement: It provides semiquantitative assessment of marrow infiltration and the degree of bone infarction. When MRI is not available, monitoring of painful acute bone crises and osteonecrosis by plain X-ray has limited value. In adult patients, we recommend DXA of the lumbar spine and left and right hips, with careful protocols designed to exclude focal disease; serial follow-up should be done using the same standardized instrument. Skeletal health may be improved by common measures, including adequate calcium and vitamin D and management of pain and orthopedic complications. Prompt initiation of specific therapy for GD is crucial to optimizing outcomes and preventing irreversible skeletal complications. Investing in safe, clinically useful, and better predictive methods for determining bone integrity and fracture risk remains a need.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Ortopedi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Orthopaedics (hsv//eng)

Nyckelord

Biomarkers
Bone Disease
Gaucher Disease
Osteonecrosis
Osteoporosis
Radiology
Therapeutics

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