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  • 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 ).
  • progressive unilateral facial atrophy
    ÁøÇ༺ Æí¾È¸éÀ§Ãà(òäú¼àõ ø¸äÔØüê×õê )
  • rapidly progressive (crescentic) glomerulonephritis
    ±Þ¼ÓÁøÇ༺»ç±¸Ã¼½Å¿°(ÐááÜòäú¼àõÞêϹô÷ãìæú)
  • rapidly progressive glomerulonephritis
    ±Þ¼ÓÁøÇ༺ »ç±¸Ã¼½Å¿°.
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  • malignant progressive histiocytoma
    ¾Ç¼º ÁøÇ༺ Á¶Á÷±¸Á¾
  • multiple progressive angioma
    ´Ù¹ß¼º ÁøÇ༺ Ç÷°üÁ¾
  • myopathic progressive muscular atrophy
    ±Ùº´Áõ¼º ÁøÇ༺ ±ÙÀ§Ãà(Áõ)(¡­òäú¼àõÐÉê×õêñø).
  • neural progressive muscular atrophy
    ½Å°æ¼º ÁøÇ༺ ±ÙÀ§Ãà(Áõ).
  • neural progressive muscular atrophy
    ½Å°æ¼º ÁøÇ༺ ±ÙÀ§Ãà(Áõ)(¡­òäú¼àõ ÐÉê×õêñø)
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    ÁøÇ༺ÀÇ(òäú¼àõ¡­), Á÷Áø(¼º)ÀÇ(òÁòä(àõ)¡­)
  • progressive bulbar palsy
    ÁøÇ༺ ±¸<¿¬¼ö>¸¶ºñ(òäú¼àõϹ<æÅâÐ> Ýö).
  • progressive cardiomyopathic lentiginosis
    ÁøÇ༺ ½É±Ùº´¼º ÈæÀÚÁõ
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  • progressive deafness
    ÁøÇà(¼º) ³­Ã»
  • progressive deafness
    ÁøÇ༺ ³­Ã»(òäú¼àõ Ññôé)
  • progressive diaphyseal dysplasia
    ÁøÇ༺ °ñ°£¼º ÀÌÇü¼º(Áõ)(òäú¼àõÍéÊÏàõì¶ û¡à÷ñø).
  • progressive diaphyseal dysplasia
    ÁøÇ༺ °ñ°£¼º ÀÌÇü¼º(Áõ)(òäú¼àõ ÍéÊÏàõ ì¶û¡à÷(ñø))
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HER hemorrhagic encephalopathy of rats; hernia
HIE human intestinal epithelium; hyper-IgE [syndrome]; hypoxic-ischemic encephalopathy
HSE herpes simplex encephalitis; hemorrhagic shock and encephalopathy
HSES hemorrhagic shock-encephalopathy syndrome
MCE medical care evaluation; military clinical engineering; multicystic encephalopathy; multiple cartila...
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PML Progressive Multifocal Leucoencephalopathy
PMR Progressive Muscle Relaxation
PME Progressive Myoclonus Epilepsy
PR Progressive Ratio
PSP Progressive supranuclear paly
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progressive muscular atrophy A serious neurologic disease that results from the progressive degeneration of the motor neurons.
(27 Sep 1997)
progressive muscular dystrophy A form of progressive muscular atrophy in which the disease begins in the muscle and not in the spinal centres.
Synonym: Erb atrophy, idiopathic muscular atrophy.
(05 Mar 2000)
progressive patient care Organization of medical and nursing care according to the degree of illness and care requirements in the hospital. The elements are intensive care, intermediate care, self-care, long-term care, and organised home care.
(12 Dec 1998)
progressive pigmentary dermatosis Chronic purpura, especially of the legs in men, spreading to form brownish patches; associated microscopically with perivascular lymphatic infiltration, diapedesis, and haemosiderosis.
Synonym: Schamberg's dermatitis.
(05 Mar 2000)
progressive pneumonia A chronic progressive, viral disease of sheep and goats manifested as maedi or visna in different parts of the world.
See: maedi, visna.
(05 Mar 2000)
progressive pneumonia virus A retrovirus (subfamily Lentivirinae) that is the cause of maedi; it is very similar to the visna virus
Synonym: medi virus, progressive pneumonia virus.
(05 Mar 2000)
progressive processes Process's that continue after they no longer serve the needs of the organism, and after cessation of the stimulus that evoked the process.
(05 Mar 2000)
progressive spinal amyotrophy A serious neurologic disease that results from the progressive degeneration of the motor neurons.
(27 Sep 1997)
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)
progressive staining A procedure in which staining is continued until the desired intensity of colouring of tissue elements is attained.
(05 Mar 2000)
progressive supranuclear palsy A disorder that is associated with nerve cell destruction and progressive lack of coordination, neck stiffness, trunk stiffness, problems with eye movement and mild dementia. Disorders that are similar include Alzheimer's disease, cerebellar dysfunction, Jakob-Creutzfeldt disease and Parkinson's disease. The cause for progressive supranuclear palsy is unknown, but is likely a degenerative nerve disorder that is somehow triggered by a viral infection. Pathologic changes include nerve cell damage and destruction of myelin sheath. There is no known cure.
(27 Sep 1997)
progressive tapetochoroidal dystrophy 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 torsion spasm A genetic, environmental, or idiopathic disorder, usually beginning in childhood or adolescence, marked by muscular contractions that distort the spine, limbs, hips, and sometimes the cranial-innervated muscles. The abnormal movements are increased by excitement and, at least initially, abolished by sleep. The musculature is hypertonic when in action, hypotonic when at rest. Hereditary forms usually begin with involuntary posturing of the foot or hand (autosomal recessive form ) or of the neck or trunk (autosomal dominant form ); both forms may progress to produce contortions of the entire body.
Synonym: progressive torsion spasm, torsion disease of childhood, torsion dystonia, Ziehen-Oppenheim disease.
(05 Mar 2000)
progressive vaccinia A severe or even fatal form of vaccinia occurring chiefly in subjects with an immunologic deficiency or dyscrasia and characterised by progressive enlargement of the initial and also of secondary lesions.
Synonym: vaccinia gangrenosa.
(05 Mar 2000)
hereditary progressive arthro-ophthalmopathy Autosomal dominant arthro-ophthalmopathy associated with progressive multiple dysplasia of the epiphyses, overtubulation of long bones, cleft lip and palate, hypermobility of joints, flattened vertebral bodies, pelvic bone deformities, and deafness.
Synonym: Stickler's syndrome.
(05 Mar 2000)
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