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    ÇѱÛ
  • steroid-induced atrophy
    ½ºÅ×·ÎÀ̵åÀ¯¹ßÀ§Ãà
  • subcutaneous atrophy
    ÇǺιØÀ§Ãà, ÇÇÇÏÀ§Ãà
  • senile atrophy
    ³ë³âÀ§Ãà
  • serous atrophy
    Àå¾×¼ºÀ§Ãà
  • simple atrophy
    ´Ü¼øÀ§Ãà
  • villous atrophy
    À¶¸ðÀ§Ãà
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 5
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  • simple atrophy
    ´Ü¼øÀ§Ãà
  • spinal muscular atrophy
    ô¼ö±ÙÀ°À§Ãà
  • steroid-induced atrophy
    ½ºÅ×·ÎÀ̵åÀ§Ãà
  • subcutaneous atrophy
    ÇÇÇÏÀ§Ãà, ÇǺιØÀ§Ãà
  • toxic atrophy
    Áßµ¶À§Ãà
  • villous atrophy
    À¶¸ðÀ§Ãà
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    ÇѱÛ
  • cystic vein
    ¾µ°³Á¤¸Æ
  • dialysis-associated cystic disease of kidney
    ½Å(ãì)ÀÇ Åõ¼®(÷âà°) ¿¬°ü¼º ³¶¼ºÁúȯ
  • hygroma, cystic
    È÷±×·Î¸¶
  • kidney,acquired cystic disease
    ÈÄõ¼º ³¶¼ºÁúȯ(ý­ô¸àõ Ò¥àõòðü´)
  • kidney,cystic diseases of medulla
    ½Å¼öÁú³¶¼ºº´º¯(½Å¼öÁúÒ¥àõܻܨ)
  • kidney,cystic dysplasia
    ³¶¼º ÀÌÇü¼º(Ò¥àõ ì¶û¡à÷)
  • medullary cystic diseaes, uremic
    ¼öÁú³¶¼ºÁúȯ(¡­Ò¥àõòðü´)
  • medullary cystic disease
    ¼öÁú³¶¼º Áúȯ(¡­Ò¥àõòðü´).
  • medullary cystic disease
    ¼öÁú³¶¼ºÁúȯ
  • multiple benign cystic epithelioma
    ´Ù¹ß¼º ¾ç¼º ³¶Á¾¼º »óÇÇÁ¾
  • pancreatic cystic fibrosis
    ÃéÀå³¶¼º ¼¶À¯Áõ(õýíôÒ¥àõ àéë«ñø)
  • papillary-cystic tumor
    À¯µÎ»ó ³¶¼ºÁ¾¾ç(êáÔéßÒ Ò¥àõðþåË)
  • restriction fragment length polymorphism,in cystic fibrosis
    ³¶¼º¼¶À¯Áõ(ÀÇ)¡­(Ò¥àõàéë«ñø¡­)
  • simple cystic kidney
    ´Ü¼ø³¶½Å(¡­³¶½Å).
  • simple cystic kidney
    ´Ü¼ø³¶½Å(¡­Ò¥ãì)
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CPCL congenital pulmonary cystic lymphangiectasia
FCH faculty contact hour; family case home; fetal cystic hygroma
ICF(M)A International Cystic Fibrosis (Mucoviscidosis) Association
MCD magnetic circular dichroism; mast-cell degranulation; mean cell diameter; mean of consecutive differ...
MLCN multilocular cystic nephroma
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DR-PLA Dentato-rubro-pallido-luysian atrophy
GA Geographic atrophy
GA Gyrate atrophy
HCSMA Hereditary Canine Spinal Muscular Atrophy
HA Hippocampal atrophy
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marantic atrophy <medicine> A wasting of flesh without fever or apparent disease; a kind of consumption; atrophy; phthisis. "Pining atrophy, Marasmus, and wide-wasting pestilence." (Milton) Marasmus senilis [L], progressive atrophy of the aged.
Origin: NL, fr. Gr, fr, to quench, as fire; pass, to die away.
Source: Websters Dictionary
(01 Mar 1998)
red 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)
gingival atrophy The exposure of root surface by an apical shift in the position of the gingiva.
(12 Dec 1998)
villous atrophy Abnormality of the small intestinal mucosa with crypt hyperplasia, resulting in flattening of the mucosa and the appearance of atrophy of villi; clinically seen in malabsorption syndromes such as sprue.
(05 Mar 2000)
central areolar choroidal atrophy A slowly progressive pigmentary degeneration in young persons; characterised by black foci closely set together and coalescent at the posterior pole and macular region.
Synonym: central areolar choroidal atrophy, central areolar choroidal sclerosis.
(05 Mar 2000)
Vulpian's atrophy Progressive spinal muscular atrophy beginning in the shoulder.
Synonym: scapulohumeral atrophy.
(05 Mar 2000)
cerebellar atrophy A degeneration of the cerebellum, particularly the Purkinje cells, as the result of abiotrophy or of toxic agents, as in alcoholism.
(05 Mar 2000)
periodontal atrophy Decrease in size and/or cellular elements of the periodontium after it has reached normal maturity.
(05 Mar 2000)
peroneal muscular atrophy A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type.
Synonym: Charcot-Marie-Tooth disease.
(05 Mar 2000)
choroidal vascular atrophy Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye.
(05 Mar 2000)
gyrate atrophy Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
(12 Dec 1998)
gyrate atrophy of choroid and retina A slowly progressive atrophy of the choriocapillaris, pigmentary epithelium, and sensory retina, with irregular confluent atrophic areas and an associated ornithinuria; autosomal recessive inheritance; due to a deficiency of ornithine d-aminotransferase.
(05 Mar 2000)
Pick's atrophy Circumscribed atrophy of the cerebral cortex.
Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy.
(05 Mar 2000)
Werdnig-Hoffmann 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)
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)
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