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"facial atrophy"¿¡ ´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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  • nerve schwannoma, facial
    ¾È¸é½Å°æÃÊÁ¾
  • nerve, facial
    ¾È¸é½Å°æ
  • nerve, proximal facial
    ±ÙÀ§¾È¸é½Å°æ
  • oblique facial cleft
    ¾ó±¼ºøÆ´»õ
  • oriented facial photogram
    ¾È¸é±Ô°Ý»çÁø(äÔØüЮ̫ÞÐòØ).
  • paralysis, facial
    ¾È¸é¸¶ºñ
  • paralysis, facial nerve
    ¾È¸é½Å°æ¸¶ºñ
  • paralysis, idiopathic facial
    Ư¹ß¼º ¾È¸é½Å°æ¸¶ºñ
  • paralysis, progressive facial
    ÁøÇ༺ ¾È¸é¸¶ºñ
  • posterior auricular nerve of facial nerve
    ¾ó±¼½Å°æÀÇ µÚ±Ó¹ÙÄû½Å°æ, ¾È¸é ½Å°æ(äÔØüãêÌè)ÀÇ ÈÄÀ̰³½Å°æ.
  • posterior auricular nerve of facial nerve
    ¾ó°óº·wÀÇ µÚõ¤aÄû½Å°æ, ¾È¸é ½Å°æ(äÔØüãêÌè)ÀÇ ÈÄÀ̰³½Å°æ. µÚ
  • posterior facial vein
    µÚ¾ó±¼Á¤¸Æ, ÈľȸéÁ¤¸Æ(ý­äÔØüð¡Øæ).
  • posterior facial vein
    µÚ¾ó°ùøþ? ÈľȸéÁ¤¸Æ(ý­äÔØüð¡Øæ).
  • postoperative facial palsy
    ¼úÈľȸé½Å°æ ¸¶ºñ
  • postoperative facial palsy
    ¼úÈľȸé½Å°æ¸¶ºñ(âúý­äÔØüãêÌèØ«Ýö)
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DOA date of admission; dead on arrival; Department of Agriculture; depth of anesthesia; differential opt...
FSHSMA facioscapulohumeral spinal muscular atrophy
GA Gamblers Anonymous; gastric analysis; gastric antrum; general anesthesia; general angiography; gener...
GAPO growth retardation, alopecia, pseudo-anodontia, and optic atrophy [syndrome]
HOGA hyperornithinemia with gyrate atrophy
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  • horizontal facial cleft
    ¼öÆò ¾È¿­
  • hypomelia-hypotrichosis-facial haemangioma syndrome
    ´ÜÁö-ºó¸ð-¾È¸é Ç÷°üÁ¾ ÁõÈıº
  • lower facial height
    ÇÏ¾È¸é °í°æ
  • mandibulo-facial dysostosis
    ÇÏ¾Ç ¾È¸é À̰ñÁõ
  • muscle of facial expression
    ¾È¸é Ç¥Á¤ ±Ù
    ´«, ÄÚ, ÀÔ ÁÖÀ§¿¡ ÀÖ´Â ±ÙÀ°À» ¾È¸é Ç¥Á¤ ±ÙÀ̶ó Çϸç, Á¾·ù¿¡´Â ±¤°æ±Ù
  • oral-facial-digital syndrome, type I
    IÇü±¸-¾È¸é-ÁöÁõÈıº
    X-¿¬°ü¼º ¿ì¼º À¯Àüº´À¸·Î¼­ ³²ÀÚ¿¡°Ô´Â Ä¡¸íÀûÀ¸·Î ±¼ÁöÁõ, ´ÙÁöÁõ, ÇÕÁöÁõ µîÀÌ Æ¯Â¡À̸ç, µÎ°³, ¾È¸é, ¼³, ±¸°³ ¹× ÇÏ¾Ç ±âÇüÀ» ¼ö¹ÝÇϰųª Áö´É ÀúÇÏ, Å»¸ðÁõ, ¾È¸é Áö·ç¸¦ ¼ö¹ÝÇÑ´Ù.
  • other facial structure
    ´Ù¸¥ ¾È¸é ±¸Á¶¹°
  • prenatal facial growth
    Ãâ»ýÀüÀÇ ¾ó±¼ ¼ºÀå
  • profile facial
    ¾È¸é Ãø¸éµµ
  • sectional facial moulage
    ºÐÇÒ¼º ¾È¸é ³³Çü
  • upper facial height
    »ó¾È¸é °í°æ
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facioscapulohumeral atrophy 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)
yellow atrophy of the liver See: acute yellow atrophy of the liver.
(05 Mar 2000)
familial 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)
Kienbock's atrophy Acute atrophy of bone in an extremity following inflammation.
(05 Mar 2000)
fatty atrophy Fatty infiltration secondary to an atrophy of the essential elements of an organ or tissue.
(05 Mar 2000)
Zimmerlin's atrophy A variety of hereditary progressive muscular atrophy in which the atrophy begins in the upper half of the body.
(05 Mar 2000)
Leber's hereditary optic atrophy Hereditary degeneration of the optic nerve and papillomacular bundle with resulting rapid loss of central vision, progressive for several weeks, then usually stationary with permanent central scotoma; age of onset is variable, most often in the third decade; more males than females are affected and transmission is cytoplasmic and strictly on the female side. Mutation on the mitochondrial chromosome involved, which presumably interacts with an X-linked mutant. This mechanism may explain the bizarre sex ratio, which differs significantly from one country to another.
(05 Mar 2000)
linear atrophy Bands of thin wrinkled skin, initially red but becoming purple and white, which occur commonly on the abdomen, buttocks, and thighs at puberty and/or during and following pregnancy, and result from atrophy of the dermis and overextension of the skin; also associated with ascites and Cushing's syndrome.
Synonym: atrophoderma striatum, lineae albicantes, lineae atrophicae, linear atrophy, stretch marks, stria, striae atrophicae, striate atrophy of skin, traction atrophy, vergeture.
(05 Mar 2000)
anterior facial vein <anatomy, vein> A continuation of the angular vein at the medial angle of the eye. It passes diagonally downward and outward, joining with the retromandibular vein below the border of the lower jaw before emptying into the internal jugular vein.
Synonym: anterior facial vein, vena facialis anterior, vena facialis.
(05 Mar 2000)
area of facial nerve <anatomy, nerve> The area in the fundus of the internal acoustic meatus superior to the transverse crest through which the facial nerve passes to enter the facial canal.
Synonym: area nervi facialis.
(05 Mar 2000)
atypical facial neuralgia Periodic pain in any region of the face, teeth, tongue, and occasionally in the occipital or shoulder area, which lasts several minutes to several days but has no trigger point and lacks the paroxysmal character of tic douloureux.
Synonym: atypical facial neuralgia.
(05 Mar 2000)
Broca's facial angle The angle formed by the intersection at the biauricular axis of lines drawn from the supraorbital point and the alveolar point.
Synonym: Broca's angles.
(05 Mar 2000)
buccal branches of facial nerve <anatomy, nerve> Motor branches of the facial nerve distributed to buccina or muscle and other muscles of facial expression below orbit and above chin.
Synonym: rami buccales nervi facialis.
(05 Mar 2000)
ganglion of facial nerve The sensory ganglion of the facial (7th cranial) nerve. The geniculate ganglion cells send central processes to the brainstem and peripheral processes to the taste buds in the anterior tongue, the soft palate, and the skin of the external auditory meatus and the mastoid process.
(12 Dec 1998)
velo-cardio-facial syndrome <syndrome> Also known as shprintzen syndrome, this more than is a congenital malformation (birth defect) syndrome with cleft palate, heart defect, abnormal face, and learning problems. The condition is therefore called the velo-cardio-facial (vcf) syndrome. (the velum is the soft palate). Other less frequent features include short stature, small-than-normal head (microcephaly), mental retardation, minor ear anomalies, slender hands and digits, and inguinal hernia. The cause is usually a microdeletion in chromosome band 22q11.2, just as in digeorge syndrome. Vcf and digeorge syndromes are different clinical expressions of essentially the same chromosome defect. Of essentially the same chromosome defect.
(12 Dec 1998)
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