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  • fatty corneal degeneration
    Áö¹æ°¢¸·º¯¼º
  • fleck corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾çÁõ
  • granular corneal dystrophy
    °ú¸³°¢¸·ÀÌ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º °¢¸·ÀÌ ¿µ¾çÁõ.
  • hereditary corneal dystrophy
    À¯Àü¼º°¢¸·ÀÌ¿µ¾çÁõ.
  • hyaline corneal degeneration
    À¯¸®Áú°¢¸·º¯¼º, È÷¾Ë¸°°¢¸·º¯¼º
  • juvenile epithelial corneal dystrophy
    ¿¬¼Ò±â°¢¸·»óÇǼ¼Æ÷ÀÌ¿µ¾ç(Áõ)
  • lattice corneal dystrophy
    °ÝÀÚ°¢¸·ÀÌ¿µ¾ç(Áõ)
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾çÁõ.
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾ç(Áõ)
  • marginal corneal degeneration
    º¯¿¬°¢¸·º¯¼º, µÑ·¹°¢¸·º¯¼º
  • marginal corneal ulcer
    º¯¿¬°¢¸·±Ë¾ç
  • microcystic corneal dystrophy
    ¼Ò³¶Æ÷°¢¸·ÀÌ¿µ¾ç(Áõ)
  • mosaic corneal degeneration
    ¸ðÀÚÀÌÅ©°¢¸·º¯¼º
  • mucinous corneal degeneration
    Á¡¾×°¢¸·º¯¼º
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anti-PNM Ab anti-peripheral nerve myelin antibody
ASPVD atherosclerotic peripheral vascular disease
BZRP benzodiazepine receptor peripheral [type]
CSPINE corticosteroid use, seropositive RA, peripheral joint destruction, involvement of cervical nerves, n...
FPR false-positive rate; finger peripheral resistance; fluorescence photobleaching recovery; N-formylpep...
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PBM Peripheral Blood Mononuclear Cells
PBMC Peripheral Blood Mononuclear Cells
PMP-22 Peripheral Myelin Protein-22
PNS Peripheral Nervous System
PTCL Peripheral T cell lymphomas
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dendritic corneal ulcer Keratitis caused by herpes simplex virus.
(05 Mar 2000)
endothelium, corneal Single layer of large flattened cells covering the surface of the cornea.
(12 Dec 1998)
epithelium, corneal The outer epithelial layer of the cornea, consisting of stratified squamous epithelium continuous with that of the conjunctiva.
(12 Dec 1998)
juvenile epithelial corneal dystrophy Epithelial dystrophy characterised by progressive cysts and opacities of the corneal epithelium, with onset in infancy.
Inheritance: autosomal dominant with incomplete penetrance.
Synonym: Meesman dystrophy.
(22 Sep 2002)
lattice corneal dystrophy A corneal dystrophy due to localised accumulation of amyloid in a reticular pattern; manifest at puberty and progressing slowly until eventually useful vision is lost; autosomal dominant inheritance.
(05 Mar 2000)
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