Traduction de «diffusion cutan » (Anglais → Français) :

diffuse cutaneous leishmaniasis | pseudolepromatous leishmaniasis | disseminated cutaneous leishmaniasis | diffuse leishmaniasis | anergic leishmaniasis | anergic cutaneous leishmaniasis

Diffuse cutaneous scleroderma

Modifiers The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes. Code Title .0 Minor glomerular abnormality Minimal change lesion .1 Focal and segmental glomerular lesions Focal and segmental:hyalinosis | sclerosis | Focal glomerulonephritis .2 Diffuse membranous glomerulonephritis .3 Diffuse mesangial proliferative glomerulonephritis .4 Diffuse endocapillary proliferative glomerulonephritis ...[+++] .5 Diffuse mesangiocapillary glomerulonephritis Membranoproliferative glomerulonephritis, types 1 and 3, or NOS .6 Dense deposit disease Membranoproliferative glomerulonephritis, type 2 .7 Diffuse crescentic glomerulonephritis Extracapillary glomerulonephritis .8 Other Proliferative glomerulonephritis NOS .9 Unspecified | Minimal change lesion | Focal and segmental:hyalinosis | sclerosis | Focal glomerulonephritis | Membranoproliferative glomerulonephritis, types 1 and 3, or NOS | Membranoproliferative glomerulonephritis, type 2 | Extracapillary glomerulonephritis | Proliferative glomerulonephritis NOS

reactive cutaneous hyperaemia | reactive cutaneous hyperemia

diffusion magnetic resonance imaging | diffusion MRI | diffusion functional magnetic resonance imaging | diffusion fMRI

diffused detector | diffused junction counter | diffused junction detector

Gougerot's disease | Gougerot's syndrome | Gougerot's trisymptomatic disease | nodular dermal allergic | allergic cutaneous angiitis | allergic cutaneous vasculitis | allergic nodular vasculitis

Progressive osseous heteroplasia (POH) is a rare genetic bone disorder with clinical characteristics of progressive extraskeletal bone formation presenting in early life with cutaneous ossification that progressively involves subcutaneous and then su

An extremely rare tumour association characterised by dual predisposition to melanoma and neural system tumours (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ