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"Dystrophy, muscular"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
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  • lattice corneal dystrophy
    °ÝÀÚ°¢¸·ÀÌ¿µ¾ç(Áõ)
  • lattice dystrophy
    °ÝÀÚÀÌ¿µ¾ç(Áõ)
  • limb girdle dystrophy
    Áö´ëÇüÀÌ¿µ¾çÁõ(ò¶Óáû¡ì¶ç½å×ñø).
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾çÁõ.
  • macular corneal dystrophy
    ¹ÝÁ¡°¢¸·ÀÌ¿µ¾ç(Áõ)
  • map-dot-fingerprint dystrophy
    ¹«´Ì°¢¸·ÀÌ¿µ¾ç(Áõ), ¹®¾ç°¢¸·ÀÌ¿µ¾ç(Áõ)
  • median nail dystrophy
    Á¤Áß¼Õ¹ßÅéÀÌ¿µ¾ç(Áõ)
  • metachromatic dystrophy
    ÀÌ¿°¼º ÀÌ¿µ¾çÁõ(ì¶æøàõì¶ç½å×ñø).
  • metachromatic dystrophy
    ÀÌ¿°¼º ÀÌ¿µ¾çÁõ(¡­ì¶ç½å×ñø)
  • microcystic corneal dystrophy
    ¼Ò³¶Æ÷°¢¸·ÀÌ¿µ¾ç(Áõ)
  • muscle dystrophy
    ±ÙÀÌ¿µ¾çÁõ.
  • muscle dystrophy
    ±ÙÀÌ¿µ¾çÁõ(¡­ì¶ç½å×ñø)
  • muscle dystrophy
    ±ÙÀÌ¿µ¾çÁõ.
  • muscle dystrophy
    ±Ù ÀÌ¿µ¾çÁõ(ÐÉì¶ç½å×ñø).
  • myotonic dystrophy
    ±Ù±äÀ强 ÀÌ¿µ¾çÁõ(ÐÉÑÌ íåàõì¶ç½å×ñø).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
MMD mass median diameter; minimum morbidostatic dose; moyamoya disease; myotonic muscular dystrophy
MyMD myotonic muscular dystrophy
NFMD National Foundation for Muscular Dystrophy
PMD Pelizaeus-Merzbacher disease; posterior mandibular depth; primary myocardial disease; private medici...
LCD coal tar solution [liquor carbonis detergens]; lattice corneal dystrophy; liquid crystal diode; loca...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
SCARMD Severe childhood autosomal recessive muscular dystrophy
CMD Congenital muscular dystrophies
CMT Congenital muscular torticollis
HCSMA Hereditary Canine Spinal Muscular Atrophy
LGMD Limb-girdle muscular dystrophies
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
thoracic-pelvic-phalangeal dystrophy Hereditary hypoplasia of the thorax, associated with pelvic skeletal abnormality.
Synonym: asphyxiating thoracic chondrodystrophy, Jeune's syndrome, thoracic-pelvic-phalangeal dystrophy.
(05 Mar 2000)
endothelial dystrophy of cornea Spontaneous loss of corneal endothelium leading to oedema of the corneal stroma and epithelium.
(05 Mar 2000)
epithelial dystrophy Corneal dystrophy affecting primarily the epithelium and its basement membrane.
See: juvenile epithelial corneal dystrophy.
(05 Mar 2000)
twenty-nail dystrophy Longitudinal ridging of all of the nails; seen in alopecia areata and lichen planus.
(05 Mar 2000)
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)
Favre's dystrophy Autosomal recessive bilateral peripheral and central retinoschisis with pigmentary degeneration of the retina, chorioretinal atrophy, vitreous degeneration, and night blindness.
Synonym: Favre's dystrophy.
(05 Mar 2000)
fingerprint dystrophy A condition wherein fine parallel lines in a fingerprint configuration area are seen in the basal epithelial layer and basement membrane of the corneal epithelium.
See: map-dot-fingerprint dystrophy.
(05 Mar 2000)
fleck dystrophy of cornea A bilateral occurrence of subtle spots in the corneal stroma; the spots vary in size and shape, and have sharp margins and clear centres; photophobia may occur; autosomal dominant inheritance.
(05 Mar 2000)
Landouzy-Dejerine dystrophy A relatively benign type of muscular dystrophy commencing in childhood and slowly progressive; characterised by wasting and weakness, sometimes asymmetrical, mainly of the muscles of the face, shoulder girdle, and arms; autosomal dominant inheritance.
Synonym: facioscapulohumeral atrophy, Landouzy-Dejerine dystrophy.
(05 Mar 2000)
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)
fuchs' endothelial dystrophy Disorder caused by loss of endothelium of the central cornea. It is characterised by hyaline endothelial outgrowths on descemet's membrane, epithelial blisters, reduced vision, and pain.
(12 Dec 1998)
Fuchs' epithelial dystrophy Epithelial oedema secondary to endothelial dystrophy of the cornea.
(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)
circular layer of muscular coat The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ).
Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae.
(05 Mar 2000)
circular layers of muscular tunics The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ).
Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae.
(05 Mar 2000)
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