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  • diffuse cerebral atrophy
    ¹Ì¸¸¼º ³úÀ§Ãà.
  • disuse atrophy
    ¹«¿ë¼º À§Ãà(ÙíéÄàõê×õê), ¹«À§À§Ãà, ºÎµ¿ÀÛ¼º À§Ãà.
  • disuse atrophy
    ºÒ¿ë¼º À§Ãà(ÝÕéÄàõê×õê), ¹«¿ë¼º À§Ãà(ÙíéÄàõê×õê), ¹«À§ À§Ãà, ºÎµ¿ÀÛ¼º À§Ãà.
  • eccentric atrophy
    Æí½É¼º À§Ãà(ø¶ãýàõê×õê), ¿ø½É¼º À§Ãà(¡­ê×õê).
  • eccentric atrophy
    ¿ø½É¼º À§Ãà(¡­ê×õê).
  • electric optic atrophy
    Àü±â½Ã½Å°æÀ§Ãà
  • endometrium,senile cystic atrophy
    ³ëÀμº ³¶¼º À§Ãà
  • essential iris atrophy
    º»Å¼ºÈ«Ã¤À§Ãà, Ư¹ß¼ºÈ«Ã¤À§Ãà
  • facial atrophy
    ¾È¸éÀ§Ãà
  • facioscapulohumeral atrophy
    ¾È¸é°ß°©»ó¿Ï(±Ù)À§Ãà(Áõ)(¡­Ì·Ë£ß¾èÓÐÉê×õêñø).
  • familial spinal muscular atrophy
    °¡Á·¼º ô¼ö¼º ±ÙÀ§Ãà(Áõ).
  • fat atrophy
    Áö¹æ À§Ãà
  • gastric atrophy
    À§¼±À§Ãà(êÖàÍê×õê).
  • gastric mucosa atrophy
    À§Á¡¸·À§Ãà.
  • geographic atrophy
    ÁöµµÇüÀ§Ãà
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AYA acute yellow atrophy
CA anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can...
CSMA chronic spinal muscular atrophy
DIDMOA diabetes insipidus-diabetes mellitus-optic atrophy [syndrome]
DIDMOAD diabetis insipidus, diabetes mellitus, otpic atrophy, deafness [syndrome]
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LCCA late cortical cerebellar atrophy
PMA progressive muscular atrophy
VA villous atrophy
BMMC Bone marrow-derived mast cells
CTMC Connective tissue mast cells
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
progressive spinal muscular atrophy One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not.
(05 Mar 2000)
scapulohumeral atrophy Progressive spinal muscular atrophy beginning in the shoulder.
Synonym: scapulohumeral atrophy.
(05 Mar 2000)
Hoffmann's muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
pulp atrophy Diminution in size and/or cellular elements of the dental pulp due to interference with the blood supply.
(05 Mar 2000)
horizontal atrophy A progressive loss of alveolar and supporting bone surrounding the teeth, beginning at the most coronal level of the bone.
Synonym: horizontal resorption.
(05 Mar 2000)
senile atrophy Wasting of tissues and organs with advancing age from decreased catabolic or anabolic processes, at times due to endocrine changes, decreased use, or ischemia.
Synonym: geromarasmus.
(05 Mar 2000)
serous atrophy A degenerative change occurring in fat cells, the fat being absorbed and its place being taken by a serous fluid.
(05 Mar 2000)
Hunt's atrophy An obsolete term for atrophy of the small muscles of the hand without sensory disturbances; two types are recognised: thenar, from compression of the thenar branch of the median nerve; hypothenar, from compression of the deep palmar branch of the ulnar nerve.
(05 Mar 2000)
spinal muscular atrophy <radiology> 2nd most common autosomal recessive disease in Caucasians, pathology, degeneration of the spinal anterior horn cells, atrophy and wasting of skeletal muscles, types, SMA I = Werdnig-Hoffman disease: rapidly progressive, SMA II = intermediate form, SMA III = Kugelberg-Welander disease: slowly progressive, uncommon adult forms, usual presentations, floppy baby, arthrogryposis, muscle weakness in infancy, diagnosis, weakness and wasting with areflexia, electrophysiology shows anterior horm cell disease, genetics, linked to chromosome 5q., neuronal apoptosis inhibitory protein (NAIP) gene, survival motor neuron (SMN) gene
(12 Dec 1998)
neuritic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
neurogenic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
neurotrophic atrophy Abnormalities of the skin, hair, nails, subcutaneous tissues and bone, caused by peripheral nerve lesions.
Synonym: neuritic atrophy, neurogenic atrophy, neurotrophic atrophy, trophic changes.
(05 Mar 2000)
striate atrophy of skin Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome.
Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture.
(05 Mar 2000)
Sudeck's atrophy Atrophy of bones, commonly of the carpal or tarsal bones, following a slight injury such as a sprain.
See: causalgia, reflex sympathetic dystrophy.
Synonym: acute reflex bone atrophy, posttraumatic osteoporosis, Sudeck's syndrome.
Origin: L. English sweat
(05 Mar 2000)
nutritional type cerebellar atrophy A restricted type of cerebellar cortical degeneration, affecting particularly the Purkinje cells of the anterior and superior vermis; probably caused by thiamin deficiency; most frequently seen in chronic alcoholics and then called alcoholic cerebellar degeneration.
(05 Mar 2000)
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