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myopathic atrophy - translation to arabic
GROUP OF DISEASES
Spinomuscular atrophy; Infantile Spinal Muscular Atrophy; Intermediate Spinal Muscular Atrophy; Spinal muscle atrophy; SMAs
myopathic atrophy
ضُمورُ الاعْتِلالِ العَضَلِيّ
spinal muscular atrophy
RARE CONGENITAL NEUROMUSCULAR DISORDER
Werdnig–Hoffman disease; Werdnig-Hoffmann disease; Werdnig-Hoffman syndrome; Kugelberg-Welander disease; Muscular atrophy, spinal; Infantile spinal muscular atrophy; Juvenile Spinal Muscular Atrophy; Adult Spinal Muscular Atrophy; SMA3; SMA1; SMA2; Spinal Muscular Atrophy; Kugelberg-Welander syndrome; Spinal muscular atrophies of childhood; Spinal muscular atrophy type 1; Spinal muscular atrophy type 3; Adult spinal muscular atrophy; Hoffmann syndrome; Hoffmann's syndrome; Survival motor neuron spinal muscular atrophy; Dubowitz disease; Werdnig–Hoffmann disease; Kugelberg–Welander disease; Werdnig–Hoffman syndrome; RG3039; Werdnig-Hoffman disease; Werdnig-Hoffmann syndrome; Proximal spinal muscular atrophy; Spinal muscular atrophy type 2; Spinal muscular atrophy type 4; Spinal muscular atrophy type 0; SMA0; 5q spinal muscular atrophy; Werdnig–Hoffmann syndrome
ضُمورٌ عَضَلِيُّ نُخاعِيُّ المَنْشَأ
atrophoderma
HUMAN DISEASE
Skin atrophy; Skin Atrophy
ضُمورُ الجِلْد
Definition
Atrophy
·vi To waste away; to Dwindle.
II. Atrophy ·vt To cause to waste away or become abortive; to starve or weaken.
III. Atrophy ·noun A wasting away from want of nourishment; diminution in bulk or slow emaciation of the body or of any part.
Wikipedia
Spinal muscular atrophies
Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body. While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.
