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"congenital ectodermal defect"¿¡ ´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®
    ÇѱÛ
  • hearing defect
    û°¢Àå¾Ö
  • heritable defect
    À¯Àü°áÇÔ
  • incongruous field defect
    ºÒÀÏÄ¡½Ã¾ß°á¼Õ
  • interatrial septal defect
    ½É¹æ»çÀ̸·°á¼Õ, ½É¹æÁ߰ݰá¼Õ
  • interventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • luteal phase defect
    Ȳ(»ö)ü±â°á¼Õ
  • migration defect
    ÀÌÁÖ°áÇÔ
  • morphologic defect
    ÇüŰáÇÔ
  • neural tube defect
    ½Å°æ°ü°á¼Õ, ½Å°æ°ü°áÇÔ
  • ostium primum defect
    ù°±¸¸Û°á¼Õ, Á¦1°ø°á¼Õ
  • outflow tract defect
    À¯Ãâ·Î°á¼Õ
  • plication defect
    ÁÖ¸§Çü¼º°áÇÔ
  • perforation defect
    ¶Õ¸²°áÇÔ, õ°ø°áÇÔ
  • perfusion defect
    °ü·ù°á¼Õ
  • scalp defect
    ¸Ó¸®µ¤°³°á¼Õ, µÎÇǰá¼Õ
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  • ¿µ¹®
    ÇѱÛ
  • interatrial septal defect
    (¢¡atrial septal defect) ½É¹æ»çÀ̸·°á¼Õ, ½É¹æÁ߰ݰá¼Õ
  • interventricular septal defect
    (¢¡ventricular septal defect) ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • migration defect
    ÀÌÁÖ°áÇÔ
  • moral defect
    µµ´ö°áÇÔ
  • morphologic defect
    ÇüŰáÇÔ
  • ostium primum defect
    ù°±¸¸Û°á¼Õ
  • outflow tract defect
    À¯Ãâ·Î°á¼Õ
  • perforation defect
    ¶Õ¸²°áÇÔ
  • perfusion defect
    °ü·ù°á¼Õ
  • plication defect
    ÁÖ¸§Çü¼º°áÇÔ
  • quantum defect
    ¾çÀÚ°á¼Õ
  • relative afferent pupillary defect
    ºñ±³µé½Å°æµ¿°ø°á¼Õ
  • retroplastic defect
    ÅðÇຯ¼º°áÇÔ
  • scalp defect
    ¸Ó¸®µ¤°³°á¼Õ, µÎÇǰá¼Õ
  • sector defect
    ºÎä²Ã½Ã¾ß°á¼Õ, ¼±Çü½Ã¾ß°á¼Õ
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    ÇѱÛ
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè).
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè)
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  • ¿µ¹®
    ÇѱÛ
  • defect of abdomen
    ¹è°áÇÔ
  • defect of alimentary tract
    ¼ÒÈ­°ü°áÇÔ
  • defect of blood vessel
    Ç÷°ü°áÇÔ
  • defect of brain
    ³ú°áÇÔ
  • defect of canalization (solid lacrimal duct)
    °üÇü¼º°áÇÔ (´«¹°°üÆó¼âÁõ)
  • defect of dental apparatus
    Ä¡¾Æ°áÇÔ
  • defect of ear
    ±Í°áÇÔ
  • defect of embryogenesis
    ¹èÀڹ߻ý°áÇÔ
  • defect of eye
    ¾È±¸°áÇÔ
  • defect of fertilization
    ¼öÁ¤°áÇÔ
  • defect of fetal membrane
    žƸ·°áÇÔ
  • defect of fusion
    À¶ÇÕ°áÇÔ
  • defect of gametogenesis
    »ý½ÄÀڹ߻ý°áÇÔ
  • defect of genitalia
    »ý½Ä±â°ü°áÇÔ
  • defect of head
    ¸Ó¸®°áÇÔ
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  • ¿µ¹®
    ÇѱÛ
  • Paraplacental chorionic defect
    ŹݰçÀ¶¸ð¸·°áÇÔ
    [¿¾ ¿ë¾î] ¹æÅ¹ÝÀ¶¸ð¸·°áÇÔ
  • Defect of fetal membrane
    žƸ·°áÇÔ
    [¿¾ ¿ë¾î] Ÿ·°áÇÔ
  • Umbilical cord defect
    ÅÈÁÙ°áÇÔ
    [¿¾ ¿ë¾î] Á¦´ë°áÇÔ
  • Retroplasty defect (Double superior vena cava)
    ÅðÇà°áÇÔ (°ãÀ§´ëÁ¤¸Æ)
    [¿¾ ¿ë¾î] ÅðÇຯ¼º°áÇÔ (°ãÀ§´ëÁ¤¸Æ)
  • Retroplasia defect
    ÅðÇຯ¼º°áÇÔ
    [¿¾ ¿ë¾î] ÅðÇຯ¼º°áÇÔ
  • Metabolic defect of nucleic acid (Purinemia)
    ÇÙ»ê´ë»ç°áÇÔ(Ç»¸°Ç÷Áõ)
    [¿¾ ¿ë¾î] ÇÙ»ê´ë»ç°áÇÔ(Ç»¸°Ç÷Áõ)
  • Hormone defect (Hermaphroditism)
    È£¸£¸ó°áÇÔ (¹ÝÀ½¾çÁõ)
    [¿¾ ¿ë¾î] È£¸£¸ó°áÇÔ (¹ÝÀ½¾çÁõ)
  • Meoitic defect
    °¨¼öºÐ¿­°áÇÔ
    [¿¾ ¿ë¾î] °¨¼öºÐ¿­±â°áÇÔ
  • Promeiotic defect
    °¨¼öºÐ¿­ÀÌÀü°áÇÔ
    [¿¾ ¿ë¾î] °¨¼öºÐ¿­Àü°áÇÔ
  • Conjunction defect
    °áÇÕ°áÇÔ
    [¿¾ ¿ë¾î] °áÇÕ°áÇÔ
  • Composition defect
    ±¸¼º°áÇÔ
    [¿¾ ¿ë¾î] ±¸¼º°áÇÔ
  • Simple morphologic defect
    ´Ü¼øÇüŰáÇÔ
    [¿¾ ¿ë¾î] ´Ü¼ø¼ºÇüÅÂÇÐÀû°áÇÔ
  • Defect of embryogenesis
    ¹èÀڹ߻ý°áÇÔ
    [¿¾ ¿ë¾î] ¹èÀÚÇü¼º°áÇÔ
  • Multiple morphologic defect
    º¹ÇÕÇüŰáÇÔ
    [¿¾ ¿ë¾î] ´Ù¹ß¼ºÇüÅÂÇÐÀû°áÇÔ
  • Defect of Integument
    ¿ÜÇǰáÇÔ
    [¿¾ ¿ë¾î] ¿ÜÇǰáÇÔ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
EEM ectodermal dysplasia, ectrodactyly, macular dystrophy [syndrome]; erythema exudativum multiforme
HEDH hypohidrotic ectodermal dysplasia-hypothyroidism [syndrome]
REEDS retention of tears, ectrodactyly, ectodermal dysplasia, and strange hair, skin and teeth [syndrome]
SCE secretory carcinoma of the endometrium; sister chromatid exchange; split hand-cleft lip/palate ectod...
ASD Atrial Septal Defect
  Types of ASD
  1. Ostium Primum ASD
  ...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
CDH Congenital Diaphragmatic Hernia
CDH Congenital Dislocation of the Hip
CDG Congenital Disorders of Glycosylation
CHD Congenital Heart Disease
CHED Congenital Hereditary Endothelial Dystrophy
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    ¼³¸í
  • congenital dysmenorrhea
    ¼±Ãµ¼º ¿ù°æ °ï¶õÁõ
  • congenital epulis
    ¼±Ãµ¼º ¿¡Çª¸®½º, ¼±Ãµ¼º Ä¡ÀºÁ¾
    Ãâ»ý ½Ã Á¸ÀçÇÏ´Â »ó¾Ç Ä¡ÀºÀÇ µ¹ÃâµÈ Á¾¹°·Î ºñƯÀÌÀûÀÌ´Ù. ½Å»ý¾Æ¿¡°Ô¸¸ ³ªÅ¸³ª´Â À¯°æ¼º Á¾¹°·Î °ú¸³ ¼¼Æ÷¼º ±Ù¸ð¼¼Æ÷Áõ°ú Á¶Á÷»óÀÌ À¯»çÇÏ¿© µÎ º´¼ÒÀÇ ±â¿øÀÌ °°´Ù´Â ÇÐÀÚµµ ÀÖ°í, ¹ß»ý ºÎÀ§°¡ ÀüÀÚ´Â »ó¾Ç ÀüÄ¡ºÎÀ̰í Ãâ»ý ½ÃºÎÅÍ Á¸ÀçÇϰí ÈÄÀÚ´Â Çô¿¡ ¹ß»ýµÇ¸ç ¾î´À ¿¬·ÉÃþ¿¡¼­³ª ¹ß»ýÇϹǷΠµÎ º´¼Ò´Â º°°³ÀÌ´Ù. ÀüÀÚ´Â Á¾¾ç Á¶Á÷¿¡¼­ °¡²û Ä¡¼º »óÇÇ Àܻ簡 ¹ß°ßµÇ¾î Ä¡¹èÀÇ ¹ßÀ° ÀÌ»óÀ¸·Î ¾ß±âµÈ´Ù°í º»´Ù. È£¹ß ºÎÀ§´Â »ó¾Ç ÀüÄ¡ºÎ·Î ±¸Çü ¶Ç´Â ³­¿øÇüÀ̸ç Á÷°æÀÌ 0.5-2.5cm Á¤µµÀÇ ¾ç¼º Áõ½Ä¹°·Î ³²¾Æº¸´Ù ¿©¾Æ¿¡¼­ 10¹èÁ¤µµ ºó¹ßÇÏ´Ù. Á¾¾çÀ» ÀÌ·ç´Â ¼¼Æ÷µéÀº Å©°í ´Ù°¢ÇüÀ̸ç, ¼¼Æ÷ÁúÀº ¿¡¿À½Å¿¡ ¿°»öµÇ¸ç °ú¸³ »óÀ̸ç ÇÙÀº ÀÛ°í ÆíÀçµÇ¾î ÀÖ´Ù.
  • congenital erythropoietic porphyria
    ¼±ÃµÀû ÀûÇ÷±¸ »ý¼º Æ÷¸£ÇǸ°Áõ
  • congenital fibrosis syndrome
    ¼±Ãµ ¼¶À¯Áõ ÁõÈıº
  • congenital fracture
    ¼±Ãµ¼º °ñÀý
  • congenital glaucoma
    ¼±Ãµ¼º ³ì³»Àå
    ³ì³»ÀåÀ̶õ ¾È¾Ð »ó½ÂÀ¸·Î ÀÎÇÏ¿© ´Ù¾çÇÑ Àå¾Ö±ºÀ» ÀÌ·ç¸ç ½Ã½Å°æ À§Ãà°ú ½Ã¾ß °á¼ÕÀ» ÃÊ·¡ÇÏ´Â ÁúȯÀÌ´Ù. ÀÌ Áß ¼±Ãµ¼º ³ì³»ÀåÀº Ãâ»ý ÈÄ 3³â À̳»¿¡ ¹ß»ýÇÏ´Â ¿µ¾Æ ³ì³»Àå°ú ±× ÀÌÈÄ¿¡ ¹ß»ýÇÏ´Â ¿¬¼Ò ³ì³»ÀåÀ¸·Î ³ª´©¾îÁø´Ù.
  • congenital granular cell epulis
    ¼±ÃµÀû °ú¸³¼¼Æ÷¼º Ä¡ÀºÁ¾
  • congenital hemolytic anemia
    ¼±Ãµ¼º ¿ëÇ÷¼º ºóÇ÷
    ÈÄõ¼º ¿ëÇ÷¼º ºóÇ÷¿¡ ´ëÀÀÇÏ¿©, ÀûÇ÷±¸ÀÇ ¼±ÃµÀûÀÎ ´ë»ç ÀÌ»ó¿¡ ÀÇÇØ ÀϾ´Â ¿ëÇ÷¼º ºóÇ÷ÀÇ ÃÑĪÀÌ´Ù. ±× ¿øÀÎÀº ¨ç ÀûÇ÷±¸ ¸· ÀÌ»ó¿¡ ÀÇÇÑ °Í
  • congenital hypothyroidism
    ¼±Ãµ¼º °©»ó¼± ±â´ÉÀúÇÏÁõ
  • congenital immunity
    ¼±Ãµ¼º ¸é¿ª
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ
  • congenital intracranial tumor
    ¼±Ãµ¼º µÎ°³³» Á¾¾ç
  • congenital leukokeratosis
    ¼±Ãµ¼º ¹é»ö °¢È­Áõ
  • congenital macroginbivae
    ¼±Ãµ¼º Ä¡Àº ºñ´ëÁõ
  • congenital megaureter
    ¼±Ãµ¼º °Å´ë¿ä°ü
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
congenital ankyloblepharon Congenital adhesion of the upper and lower eyelid by bands of tissue.
Synonym: filiform adnatum.
Origin: ankylo-+ G. Blepharon, eyelid
(05 Mar 2000)
congenital antithrombin III deficiency Antithrombin III is a protein which stimulates the removal of blood clots in the bloodstream. Small blood clots form normally within the bloodstream, but are normally dissolved via the bodys antithrombin III. The deficiency of antithrombin III will result in an increased risk for blood clot formation causing organ damage. This is an inherited as a autosomal dominant trait.
Inheritance: autosomal dominant.
(27 Sep 1997)
congenital aplasia of thymus diGeorge syndrome
congenital aplastic anaemia <haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant.
Origin: Gr. Haima = blood
(13 Nov 1997)
congenital atonic pseudoparalysis Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves.
Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome.
An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive).
(05 Mar 2000)
congenital baldness Absence of all hair at birth, associated with psychomotor epilepsy; autosomal dominant inheritance.
Synonym: congenital baldness, hypotrichiasis.
(05 Mar 2000)
congenital bronchiectasis Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Although rarely congenital, it is most often an acquired condition in childhood.
(27 Sep 1997)
congenital cardiomyopathy <radiology> Endocardial fibroelastosis, myocarditis, glycogen storage disease (Pompe's), anomalous origin of left coronary artery from pulmonary artery
(12 Dec 1998)
congenital cataract A cataract or clouding or the lens of the eye, that occurs in the foetus at some time during pregnancy. Children with Down's syndrome and galactosaemia have an increased incidence of congenital cataracts.
Treatment includes cataract removal and the insertion of an artificial lens.
(27 Sep 1997)
congenital cerebellar atrophy Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate.
(05 Mar 2000)
congenital cerebral aneurysm Localised dilation of a cerebral vessel; usually a berry aneurysm.
(05 Mar 2000)
congenital choreoathetosis A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia.
Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome.
(05 Mar 2000)
congenital clasped thumb with mental retardation See: Clasped thumbs and mental retardation.
(12 Dec 1998)
congenital conus A congenital inferior crescent on the choroid at the edge of the optic disk; not associated with myopia.
Synonym: congenital conus.
(05 Mar 2000)
congenital diaphragmatic hernia Absence of the pleuroperitoneal membrane (usually on the left) or an enlarged Morgagni's foramen which allows protrusion of abdominal viscera into the chest.
Synonym: Bochdalek's hernia.
(05 Mar 2000)
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