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"fatty atrophy"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
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  • hereditary optic atrophy
    À¯Àü¼º ½Ã½Å°æÀ§Ãà.
  • hereditary optic atrophy
    À¯Àü¼º½Ã½Å°æÀ§Ãà.
  • hypothenar atrophy
    ¼ÒÁö±¸ À§Ãà(á³ò¦Ï¹êÍõê).
  • hypothenar atrophy
    ¼ÒÁö±¸À§Ãà.
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü ±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile muscular atrophy =Werdnig-Hoffmann disease
    ¿µ¾ÆÇü±ÙÀ§ÃàÁõ(?ä®û¡ÐÉê×õêñø).
  • infantile progressive spinal muscular atrophy
    ¿µ¾ÆÁøÇ༺ ô¼ö¼º ±ÙÀ§Ãà(Áõ).
  • iris atrophy
    ȫäÀ§Ãà
  • ischemic optic atrophy
    ÇãÇ÷½Ã½Å°æÀ§Ãà
  • juvenile muscular atrophy
    ¿¬¼Ò¼º ±ÙÀ§Ãà(¡­ÐÉê×õê).
  • juvenile progressive muscular atrophy
    ¿¬¼Ò¼º ÁøÇ༺ ±ÙÀ§ÃàÁõ(¡­òäú¼àõÐÉê× õêñø).
  • lactation atrophy
    ¼öÀ¯À§Ãà(¡­ê×õê).
  • lacunar optic atrophy
    ÇØ¸é½Ã½Å°æÀ§Ãà
  • leaping atrophy
    ºñ¿ùÀ§Ãà
  • lobar atrophy
    ³ú¿±À§Ãà(Òàç¨ê×õê).
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SMA sequential multiple analysis or analyzer; sequential multichannel autoanalyzer; simultaneous multich...
SPMA spinal progressive muscular atrophy
STVA subtotal villose atrophy
SVA selective vagotomy and antrectomy; selective visceral angiography; sequential ventriculoatrial [paci...
SYA subacute yellow atrophy
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FAAH Fatty acid amide hydrolase
FABP Fatty acid binding protein
FAEE Fatty acid ethyl ester
FAO Fatty acid oxidation
FAS Fatty acid synthase
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compensatory atrophy Atrophy especially of an endocrine organ as a result of its function being assumed by a new source of hormone.
(05 Mar 2000)
congenital cerebellar atrophy Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate.
(05 Mar 2000)
multiple system atrophy A name grouping together the four cerebral degenerative diseases of olivopontocerebellar atrophy, shy-drager syndrome, striatonigral degeneration, and one form of parkinson disease, considering them different forms of the same disease process.
(12 Dec 1998)
muscular atrophy Derangement in size and number of muscle fibres occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.
(12 Dec 1998)
muscular atrophy, spinal Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations.
(12 Dec 1998)
myopathic atrophy Muscular atrophy caused by a primary disorder of muscle.
(05 Mar 2000)
postmenopausal atrophy Atrophy following menopause, as of the genital organs.
(05 Mar 2000)
cyanotic atrophy Atrophy due to destruction of the parenchymatous cells of an organ as a consequence of chronic venous congestion.
Synonym: red atrophy.
(05 Mar 2000)
cyanotic atrophy of the liver A sequela of longstanding hepatic congestion due to high pressure in the right atrium as in chronic constrictive pericarditis and severe, protracted right ventricular failure.
(05 Mar 2000)
pressure atrophy The wasting of hard or soft tissue resulting from excessive pressure applied to tissue by a denture base.
(05 Mar 2000)
primary idiopathic macular atrophy Atrophoderma in which the skin becomes bag like and wrinkled.
Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin.
Origin: G. Anetos, relaxed, + derma, skin
(05 Mar 2000)
primary macular atrophy of skin Atrophoderma in which the skin becomes bag like and wrinkled.
Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin.
Origin: G. Anetos, relaxed, + derma, skin
(05 Mar 2000)
progressive choroidal atrophy An x chromosome-linked abnormality characterised by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness.
(12 Dec 1998)
progressive circumscribed cerebral atrophy Circumscribed atrophy of the cerebral cortex.
Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy.
(05 Mar 2000)
progressive infantile spinal 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)
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