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1000 Titel
  • Hip pathologies in mucopolysaccharidosis type III
1000 Autor/in
  1. Breyer, Sandra |
  2. Vettorazzi, Eik |
  3. Schmitz, Leonie |
  4. Gulati, Amit |
  5. von Cossel, Katharina Maria |
  6. Spiro, Alexander |
  7. Rupprecht, Martin |
  8. Stuecker, Ralf |
  9. Muschol, Nicole Maria |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-03-19
1000 Erschienen in
1000 Quellenangabe
  • 16(1):201
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13018-021-02340-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977579/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Mucopolysaccharidosis type III (MPS III) comprises a group of rare lysosomal storage diseases. Although musculoskeletal symptoms are less pronounced than in other MPS subtypes, pathologies of hip and spine have been reported in MPS III patients. The purpose of this study was to describe hip pathologies and influencing parameters in MPS III patients.!##!Methods!#!A retrospective chart review was performed for 101 MPS III patients. Thirty-two patients met the inclusion criteria of enzymatically or genetically confirmed diagnosis and anteroposterior radiograph of the hips. Modified Ficat classification, Wiberg's center-edge angle, and Reimer's migration percentage were measured.!##!Results!#!The mean age at data assessment was 11.0 years (SD 5.7). Osteonecrosis of the femoral head was observed in 17/32 patients. No statistically significant association was found between these changes and age, sex, or MPS III subtype. Patients with a severe phenotype showed significantly higher rates of osteonecrosis (14/17) than patients with an intermediate phenotype. Hip dysplasia was present in 9/32 patients and was significantly associated with osteonecrosis of the femoral head (p = 0.04).!##!Conclusions!#!The present study demonstrates a high rate of hip pathologies in MPS III patients. Hip dysplasia and severe phenotype were significantly correlated with osteonecrosis of the femoral head. Therefore, radiographs of the hips are highly recommended in baseline and follow-up assessments of MPS III patients.!##!Trial registration!#!Retrospectively registered.
1000 Sacherschließung
lokal Femur Head Necrosis/pathology [MeSH]
lokal Dysostosis multiplex
lokal Mucopolysaccharidosis type III
lokal Hip/diagnostic imaging [MeSH]
lokal Hip Dislocation/pathology [MeSH]
lokal Male [MeSH]
lokal Hip/pathology [MeSH]
lokal Mucopolysaccharidoses/pathology [MeSH]
lokal Pain
lokal Sanfilippo syndrome
lokal Hip Dislocation/etiology [MeSH]
lokal Child [MeSH]
lokal Research Article
lokal Adolescent [MeSH]
lokal Female [MeSH]
lokal Osteonecrosis
lokal Radiography [MeSH]
lokal Adult [MeSH]
lokal MPS
lokal Humans [MeSH]
lokal Skeletal disease
lokal Retrospective Studies [MeSH]
lokal Hip dysplasia
lokal Mucopolysaccharidoses/diagnostic imaging [MeSH]
lokal Femur Head Necrosis/etiology [MeSH]
lokal Femoral head
lokal Young Adult [MeSH]
lokal Skeletal dysplasia
lokal Mucopolysaccharidoses/complications [MeSH]
lokal Child, Preschool [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-1122-0266|https://frl.publisso.de/adhoc/uri/VmV0dG9yYXp6aSwgRWlr|https://frl.publisso.de/adhoc/uri/U2NobWl0eiwgTGVvbmll|https://frl.publisso.de/adhoc/uri/R3VsYXRpLCBBbWl0|https://frl.publisso.de/adhoc/uri/dm9uIENvc3NlbCwgS2F0aGFyaW5hIE1hcmlh|https://frl.publisso.de/adhoc/uri/U3Bpcm8sIEFsZXhhbmRlcg==|https://frl.publisso.de/adhoc/uri/UnVwcHJlY2h0LCBNYXJ0aW4=|https://frl.publisso.de/adhoc/uri/U3R1ZWNrZXIsIFJhbGY=|https://frl.publisso.de/adhoc/uri/TXVzY2hvbCwgTmljb2xlIE1hcmlh
1000 Hinweis
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1000 Label
1000 Dateien
  1. Hip pathologies in mucopolysaccharidosis type III
1000 Objektart article
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1000 @id frl:6463463.rdf
1000 Erstellt am 2023-11-15T18:47:16.717+0100
1000 Erstellt von 322
1000 beschreibt frl:6463463
1000 Zuletzt bearbeitet 2023-11-30T21:42:59.414+0100
1000 Objekt bearb. Thu Nov 30 21:42:59 CET 2023
1000 Vgl. frl:6463463
1000 Oai Id
  1. oai:frl.publisso.de:frl:6463463 |
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