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  • progressive spinal amyotrophy
    ÁøÇ༺ ô¼ö¼º ±ÙÀ§ÃàÁõ(òäú¼àõ ô±âÐàõ ÐÉê×õêñø)
  • progressive subcortical encephalopathy
    ÁøÇ༺ ÇÇÁúÇϳúÀå¾Ö<³úÁõ>(¡­ù«òõù» Òàî¡äô<Òàñø>).
  • progressive subcortical encephalopathy
    ÁøÇ༺ ÇÇÁúÇϳúÀå¾Ö<³úÁõ>(òäú¼àõ ù«òõù»Òàî¡äô<Òàñø>)
  • progressive supranuclear palsy
    ÁøÇ༺ Çٻ󸶺ñ(òäú¼àõú·ß¾ Ýö).
  • progressive supranuclear palsy
    ÁøÇ༺ »óÇÙ¸¶ºñ(Çٻ󸶺ñ)(òäú¼àõ ß¾ú·Ø¦Ýö(ú·ß¾Ø¦Ýö))
  • progressive symmetric erythrokeratodermia
    ÁøÇ༺ ´ëμº È«»ö °¢ÇÇÁõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å °æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(Ìãûùñø)
  • progressive systemic sclerosis
    ÁøÇà(¼º) Àü½Å°æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å°æÈ­Áõ
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(òäú¼àõ îñãóàõ Ìãûùñø)
  • progressive systemic sclerosis
    ÁøÇ༺ Àü½Å¼º °æÈ­Áõ(òäú¼àõîñãóàõÌãûùñø).
  • progressive thrombus
    ÁøÇ༺ Ç÷Àü(¡­úìîû).
  • progressive thrombus
    ÁøÇ༺ Ç÷Àü(òäú¼àõ úìîû)
  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõø¸äÔØüê×õê ).
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  • progressive multifocal leukoencephalopathy
    ÁøÇ༺ ´ÙÃÊÁ¡¼º ¹éÁú³úº´Áõ(òäú¼àõ Òýõ¥ïÇàõ ÛÜòõÒàÜ»ñø)
  • progressive muscle dystrophy
    ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ(òäú¼àõÐÉì¶ç½å×ñø).
  • progressive muscle dystrophy
    ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ(òäú¼àõ ì¶ç½å×ñø)
  • progressive myoclonic epilepsies
  • progressive myopathy
    ÁøÇ༺ ±Ùº´Áõ(¡­ÐÉÜ»ñø).
  • progressive myopathy
    ÁøÇ༺ ±Ùº´Áõ(òäú¼àõ ÐÉÜ»ñø)
  • progressive myopia
    ÁøÇ༺ ±Ù½Ã(òäú¼àõ ÐÎãÊ) ¾Æµ¿ÀÇ
  • progressive neural muscular atrophy
    ÁøÇ༺ ½Å°æ¼º ±ÙÀ§Ãà(¡­ãêÌèàõÐÉê×õê).
  • progressive neural muscular atrophy
    ÁøÇ༺ ½Å°æ¼º ±ÙÀ§Ãà(òäú¼àõ ãêÌèàõ ÐÉê×õê)
  • progressive nodular fibrosis of the skin
    ÁøÇ༺ °áÀý ÇǺΠ¼¶À¯Áõ
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ÇÙ¼º¾È±Ù¸¶ºñ.
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ ÇÙ¼º ¾È±Ù¸¶ºñ(òäú¼àõ ú·àõ äÑÐÉØ¦Ýö)
  • progressive nuclear ophthalmoplegia
    ÁøÇ༺ÇÙ¼º¾È±Ù¸¶ºñ
  • progressive ophtalmoplegia
    ÁøÇ༺ ¾È±Ù ¸¶ºñ(òäú¼àõ äÑÐÉØ¦Ýö)
  • progressive pigmentary dermatosis
    ÁøÇ༺ »ö¼Ò¼º ÇǺÎÁõ
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EPR early progressive resistance; electron paramagnetic resonance; electronic patient record; electrophr...
GFD gingival fibromatosis-progressive deafness [syndrome]; gluten-free diet
MDP manic-depressive psychosis; maximum diastolic potential; maximum digital pulse; methylene diphosphat...
PADUA progressive augmentation by dilating the urethra anterior
PAE progressive assistive exercise
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PEO Progressive external ophthalmoplegia
PME Progressive myoclonic epilepsy
PRA Progressive retinal atrophy
prcd Progressive rod-cone degeneration
R.P.P. Rapidly Progressive Periodontitis
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supranuclear palsy, progressive A progressive neurological disease usually of the fifth decade characterised by supranuclear ophthalmoplegia especially paralysis of downward gaze, pseudobulbar palsy, gait disturbance, dysathria, truncal dystonia, memory and personality deterioration, and dementia.
(12 Dec 1998)
diaphyseal dysplasia, progressive Progressive thickening of diaphyseal cortex of long bones.
(12 Dec 1998)
infantile progressive 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)
ophthalmoplegia, chronic progressive external One of the mitochondrial encephalomyopathies characterised by slowly progressive paralysis of the extraocular muscles. Muscle biopsies disclose the characteristic ragged red fibres and large numbers of mitochondria with deleted DNA.
(12 Dec 1998)
ovine progressive pneumonia A chronic, progressive, contagious interstitial pneumonitis of sheep in Europe and the U.S. Caused by a "slow virus" (family Lentiviridae); it is now believed that maedi and visna are two histopathological and clinical manifestations of the same viral infection.
Synonym: ovine progressive pneumonia.
Origin: Icelandic, dyspnea
(05 Mar 2000)
traumatic progressive encephalopathy A chronic progressive brain damage resulting from multiple brain injuries, e.g., dementia pugilistica.
(05 Mar 2000)
essential progressive atrophy of iris Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years.
(05 Mar 2000)
lenticular progressive degeneration <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure.
Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common.
Inheritance: autosomal recessive.
(27 Sep 1997)
leukoencephalopathy, progressive multifocal Rare demyelinating disease of the central nervous system which develops in immunocompromised patients secondary to lymphoproliferative disease, immunosuppressive therapy, autoimmune disorders, or aids. It is caused by the jc virus, a polyomavirus.
(12 Dec 1998)
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