Traduction de «histiocytosis x syndrome » (Anglais → Néerlandais) :

TERMINOLOGIE

histiocytosis X | histiocytosis X syndrome | Langerhans' cell granulomatosis | Langerhans cell histiocytosis | LCH [Abbr.]
histiocytose-X | Langerhans Cel Histiocytose | LHC [Abbr.]

Abt-Letterer-Siwe disease | Abt-Letterer-Siwe syndrome | acute disseminated histiocytosis X | infectious reticulo-endotheliosis | Letterer-Siwe disease | multifocal multisystem Langerhans cell histiocytosis
syndroom van Abt-Siwe-Letterer

DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency
ziekte van Niemann-Pick

Other histiocytosis syndromes
overige histiocytosesyndromen

Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma
reticulohistiocytoom (reuscel) | sinushistiocytose met massale lymfadenopathie | xanthogranuloom

Arthropathy in:leukaemia (C91-C95+) | malignant histiocytosis (C96.1+) | multiple myeloma (C90.0+)
artropathie bij | leukemie (C91-C95) | artropathie bij | maligne histiocytose (C96.8) | artropathie bij | multipel myeloom (C90.0)

Benign cephalic histiocytosis
goedaardige cefalische histiocytose

A form of non-Langerhans cell histiocytosis with characteristics of cutaneous presentation of solitary or disseminated yellow to orange-brown papular or papulonodular, noncoalescent, asymptomatic skin lesions located predominantly on the head, neck,
papulair xanthoom

A rare benign non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, w
erfelijke progressieve mucineuze histiocytose

building safety [ SBS | sick building syndrome ]
veiligheid van gebouwen [ hygiënevoorschriften voor gebouwen ]

TRADUCTIONS EN CONTEXTE

List of pilot European Reference Networks for Rare Diseases · Dyscerne: European Network of Centres of Reference for Dysmorphology · ECORN CF: European Centres of Reference Network for Cystic Fibrosis · PAAIR: Patient Associations and Alpha1 International Registry, · EPNET European Porphyria Network, · EN-RBD European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network · NEUROPED: European Network of Reference for Rare Paediatric Neurological Diseases · EURO HISTIO NET: A reference network for Langerhans cell histiocytosis and associated syndrome in EU · TAG: Together Against Genodermatoses · CARE NMD: Dissemination and Implementation of the Standards of Care for Duchene muscular Dystrophy in Europe
Overzicht van Europese proefreferentienetwerken inzake zeldzame ziekten · Dyscerne: Europees netwerk van referentiecentra voor dysmorfologie (European Network of Centres of Reference for Dysmorphology) · ECORN CF: Europees netwerk van referentiecentra voor taaislijmziekte (European Centres of Reference Network for Cystic Fibrosis) · PAAIR: Internationaal register van patiëntenverenigingen en Alpha1 (Patient Associations and Alpha1 International Registry) · EPNET: Europees porfyrienetwerk · EN-RBD: Europees Netwerk voor zeldzame bloedaandoeningen, netwerk van Hodgkin lymfoom bij kinderen (European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network) · NEUROPED: Europees netwerk voor zeldzame neurologische aandoeningen bij kinderen (European Network of Reference for Rare Paediatric Neurological Diseases) · EURO HISTIO NET: Een referentienetwerk voor Langerhanscelhistiocytose en aanverwante syndromen in de EU · TAG: Samen tegen genodermatose (Together Against Genodermatoses) · CARE NMD: Verspreiding en toepassing van de zorgstandaarden voor spierdystrofie van Duchenne in Europa