Traduction de «Concentric sclerosis » (Anglais → Français) :

Concentric sclerosis [Baló]

Balo concentric sclerosis

multiple sclerosis [ MS | disseminated multiple sclerosis | disseminated sclerosis | focal sclerosis | insular sclerosis ]

multiple sclerosis | MS | disseminated sclerosis | focal sclerosis | insular sclerosis

Pelizaeus-Merzbacher disease [ Merzbacher-Pelizaeus disease | familial centrolobar sclerosis | Pelizaeus-Merzbacher sclerosis ]

athlete with multiple sclerosis [ multiple sclerosis athlete | MS athlete ]

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

A rare urogenital disease characterized by the appearance of flu-like symptoms (fever, extreme fatigue, myalgia, itchy burning eyes, nasal congestion/rhinorrhea), as well as mood changes, irritability and concentration, memory and attention difficult

A rare genetic congenital hypothyroidism disorder with characteristics of mild global developmental delay in childhood, short stature, delayed bone age and abnormal thyroid and selenium levels in serum (high total and free T4 concentrations, low T3,

S. Considering that people with Multiple Sclerosis are frequently disappointed with the level of understanding and expertise of health care professionals who deal with their problems, and that a more positive approach is often required towards them which concentrates also on what they can achieve as individuals rather than focusing exclusively on their problems;

S. considering that people with multiple sclerosis are frequently disappointed with the level of understanding and expertise of health care professionals who deal with their problems, and that a more positive approach is often required towards them which also concentrates on what they can achieve as individuals rather than focusing exclusively on their problems,