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Dictionnaire français - anglais

syndrome d'Adair-Dighton

Adair Dighton syndrome

santé - iate.europa.eu

brittle bone syndrome

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brittle bone disease

santé - iate.europa.eu
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A courtroom diagnosis: countering the defense of temporary brittle bone disease and mild oi... In some jurisdictions, judges are allowing defense medical experts to testify that infants have not been abused, but instead suffer from a mild form of Osteogenesis Imperfecta (OI) or a purported variant of OI, Temporary Brittle Bone Disease (TBBD)....
général - core.ac.uk - PDF: ecollections.law.fiu.edu
Long-term follow-up of children thought to have temporary brittle bone disease... One controversial postulated cause is temporary brittle bone disease, first described in 1990.Methods:...
 PDF: doaj.org

glass bone disease

santé - iate.europa.eu

osteogenesis imperfecta

santé - iate.europa.eu
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Severe osteogenesis imperfecta in cyclophilin b–deficient miceOsteogenesis Imperfecta (OI) is a human syndrome characterized by exquisitely fragile bones due to osteoporosis....
santé - core.ac.uk - PDF: citeseerx.ist.psu.edu

osteogenesis imperfecta tarda

santé - iate.europa.eu
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Osteogenesis imperfecta in twenty-three members of a kindred with heritable features contributed by a non-specific skeletal... The second variety, osteogenesis imperfecta tarda (OIT) is better known, its manifestations may be so mild that blue sclerae may be the only evidence of the condition....
général - core.ac.uk - PDF: qjmed.oxfordjournals.org
Left ventricular rupture after mitral valve replacement in a patient with osteogenesis imperfecta tarda.We describe the case of a patient with osteogenesis imperfecta tarda (Lobstein's syndrome) and mitral valve insufficiency....
 PDF: www.pubmedcentral.nih.gov

osteogenesis imperfecta type I

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Blegvad-Haxthausen syndrome

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Lobstein’s disease

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Lobstein disease

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Publications scientifiques

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Sequential traumatic corneal open globe rupture in a patient with osteogenesis imperfecta type iPurpose: To report a case of sequential open globe rupture in a young patient with osteogenesis imperfecta type I following minor accidental blunt injury....
santé / produit animal / politique agricole - core.ac.uk - PDF: doaj.org
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Mutations linked to the pro alpha 2(i) collagen gene are responsible for several cases of osteogenesis imperfecta type i.We have analysed six South African families with osteogenesis imperfecta type I using three DNA polymorphisms associated with the pro alpha 2(I) collagen gene....
général - core.ac.uk - PDF: www.pubmedcentral.nih.gov

Synonymes et termes associés français

maladie de Lobstein

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ostéopsathyrose

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syndrome d'Adair-Dighton

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dysplasie périostale

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ostéogénèse imparfaite

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ostéogenèse imparfaite tardive

[...]

syndrome de Blegvad-Haxthausen

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maladie des os de verre

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syndrome

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Syndrome

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Exemples français - anglais

syndrome

syndrome
santé - iate.europa.eu


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