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"afferent pupillary 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
  • 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
  • synthesis defect
    ÇÕ¼º°áÇÔ
  • sector defect
    ºÎä²Ã½Ã¾ß°á¼Õ, ¼±Çü½Ã¾ß°á¼Õ
  • sensory defect
    °¨°¢°á¼Õ
  • separation defect
    ºÐ¸®°áÇÔ
  • septal defect
    »çÀ̸·°á¼Õ, Á߰ݰá¼Õ
  • septation defect
    »çÀ̸·Çü¼º°á¼Õ, Áß°ÝÇü¼º°á¼Õ
  • skull bone defect
    ¸Ó¸®»À°á¼Õ, µÎ°³°ñ°á¼Õ
  • ventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
  • ¿µ¹®
    ÇѱÛ
  • 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
  • retroplastic defect
    ÅðÇຯ¼º°áÇÔ
  • scalp defect
    ¸Ó¸®µ¤°³°á¼Õ, µÎÇǰá¼Õ
  • sector defect
    ºÎä²Ã½Ã¾ß°á¼Õ, ¼±Çü½Ã¾ß°á¼Õ
  • sensory defect
    °¨°¢°á¼Õ
  • separation defect
    ºÐ¸®°áÇÔ
  • septal defect
    »çÀ̸·°á¼Õ, Á߰ݰá¼Õ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
  • ¿µ¹®
    ÇѱÛ
  • gametic defect
    »ý½ÄÀÚ°áÇÔ
  • gene defect
    À¯ÀüÀÚ°á¼Õ<--°á¿©>
  • genetic defect
    À¯ÀüÀû °áÇÔ(¡­ÌÀùè).
  • genetic defect
    À¯ÀüÀÚ°áÇÔ
  • genetic defect
    À¯ÀüÀû °áÇÔ.
  • growth defect
    ¼ºÀå°áÇÔ
  • hearing defect
    û·ÂÀå¾Ö
  • heart defect
    ½ÉÀå°áÇÔ
  • heart septal defect
    ½ÉÁ߰ݰá¼Õ(Áõ)(ãýñḛ́ÌÀáßñø).
  • heritable defect
    À¯Àü°áÇÔ
  • high ventricular septal defect
    °íÀ§½É½ÇÁ߰ݰá¼Õ.
  • placental defect
    ŹݰáÇÔ
  • plication defect
    ÁÖ¸§Çü¼º°áÇÔ
  • plication defect (schistomyelia)
    ÁÖ¸§Çü¼º°áÇÔ (ô¼ö°¥¸²Áõ)
  • postnatal defect
    Ãâ»ýÀÌÈİáÇÔ
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  • ¿µ¹®
    ÇѱÛ
  • aortic septal defect
    ´ëµ¿¸ÆÁ߰ݰá¼Õ(ÓÞÔÑØæñḛ́ÌÀáß).
  • aortic septal defect
    ´ëµ¿¸ÆÁ߰ݰá¼Õ(ÓÞÔÑØæñḛ́ÌÀáß).
  • aorticopulmonary septal defect
    ´ëµ¿¸ÆÆóµ¿¸ÆÁ߰ݰá¼Õ(¡­ñḛ́ÌÀáß).
  • aorticopulmonary septal defect
    ´ëµ¿¸ÆÆóµ¿¸ÆÁ߰ݰá¼Õ(¡­ñḛ́ÌÀáß).
  • aortopulmonary septal defect
    ´ëµ¿¸ÆÆóµ¿¸ÆÁ߰ݰá¼Õ.
  • aortopulmonary septal defect
    ´ëµ¿¸ÆÆóµ¿¸ÆÁ߰ݰá¼Õ.
  • atrial septal defect
    ½É¹æÁ߰ݰá¼Õ(Áõ)(¡­ñḛ́ÌÀáßñø).
  • atrial septal defect
    ½É¹æ»çÀ̸·°á¼Õ
  • atrial septal defect
    ½É¹æÁ߰ݰá¼Õ(Áõ)(¡­ñḛ́ÌÀáßñø)
  • atrioventricular canal defect
    ¹æ½Ç°ü°á¼Õ(¡­Î·ÌÀáß).
  • atrioventricular septal defect
    ¹æ½ÇÁ߰ݰá¼Õ(Áõ).
  • atrioventricular septal defect
    ¹æ½ÇÁ߰ݰá¼Õ(Áõ)
  • atroventricular septal defect
    ¹æ½ÇÁ߰ݰá¼Õ(Û®ãøñḛ́ÌÀáß)
  • auditory defect
    û°á¼Õ
  • basic defect
    ±âº»Àû °á¼Õ
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  • ¿µ¹®
    ÇѱÛ
  • Prenatal defect
    Ãâ»ýÀÌÀü°áÇÔ
    [¿¾ ¿ë¾î] Ãâ»ýÀü°áÇÔ
  • Postnatal defect
    Ãâ»ýÀÌÈİáÇÔ
    [¿¾ ¿ë¾î] Ãâ»ýÈİáÇÔ
  • Metabolic defect of carbohydrate (Galactosemia)
    ź¼öÈ­¹°´ë»ç°áÇÔ(°¥¶ôÅä¿À½ºÇ÷Áõ)
    [¿¾ ¿ë¾î] ź¼öÈ­¹°´ë»ç°áÇÔ(°¥¶ôÅä¿À½ºÇ÷Áõ)
  • Placental defect
    ŹݰáÇÔ
    [¿¾ ¿ë¾î] ŹݰáÇÔ
  • 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
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
VSD Ventricular Septal Defect
  ? Types of VSD
    1. Subpulmonic(=...
APSD aorticopulmonary septal defect
AREDYLD acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes [syndrome]
AVSD atrioventricular septal defect
COVESDEM costovertebral segmentation defect with mesomelia [syndrome]
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • myelinated afferent
    À¯¼öÃÊ ±¸½É ½Å°æ
  • myelinated afferent inhibition
    À¯¼öÃÊ ±¸½É¼º ¾ïÁ¦
  • myelinated cutaneous afferent
    À¯¼öÃÊ ÇǺΠ±¸½É ½Å°æ
  • myelinated non-nociceptive afferent
    À¯¼öÃÊ ºñÄ§ÇØ¼ö¿ë¼º ±¸½É ½Å°æ, À¯¼öÃÊ ºñÀ¯Çؼö¿ë¼º ±¸½É ½Å°æ
  • myelinated primary afferent
    ÀÏÂ÷ À¯¼öÃÊ ±¸½É ½Å°æ
  • nociceptive afferent input
    Ä§ÇØ ¼ö¿ë¼º ±¸½É ÀÔ·Â, À¯ÇØ ¼ö¿ë¼º ±¸½É ÀÔ·Â
  • nociceptive primary afferent
    Ä§ÇØ ¼ö¿ë¼º ÀÏÂ÷ ±¸½É ½Å°æ, À¯ÇØ ¼ö¿ë¼º ÀÏÂ÷ ±¸½É ½Å°æ
  • non-nociceptive A delta C primary afferent
    ºñÄ§ÇØ ¼ö¿ë¼º A µ¨Å¸ C ÀÏÂ÷ ±¸½É ½Å°æ, ºñÀ¯ÇØ ¼ö¿ë¼º A µ¨Å¸ C ÀÏÂ÷ ±¸½É ½Å°æ
  • non-nociceptive myelinated afferent
    ºñÄ§ÇØ ¼ö¿ë¼º À¯¼ö ±¸½É ¼¶À¯, ºñÀ¯ÇØ ¼ö¿ë¼º À¯¼ö ±¸½É ¼¶À¯
  • non-nociceptive myelinated primary afferent
    ºñÄ§ÇØ ¼ö¿ë¼º ÀÏÂ÷ ±¸½É ¼¶À¯, ºñÀ¯ÇØ ¼ö¿ë¼º ÀÏÂ÷ ±¸½É ¼¶À¯
  • primary afferent axon
    ÀÏÂ÷ ±¸½É¼º Ãà»è
  • primary afferent cell body
    ÀÏÂ÷ ±¸½É¼º ¼¼Æ÷ü
  • primary afferent fiber
    ÀÏÂ÷ ±¸½É ¼¶À¯
  • primary afferent nociceptive transmitter
    ÀÏÂ÷ ±¸½É À¯ÇØ ¼ö¿ë¼º Àü´Þ ¹°Áú
  • primary afferent nociceptor input
    ÀÏÂ÷ ±¸½É¼º Ä§ÇØ¼ö¿ëü ÀÔ·Â, ÀÏÂ÷ ±¸½É¼º À¯Çؼö¿ë±â ÀÔ·Â
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
defect, enzyme An abnormality in the protein (enzyme) important in catalyzing a normal biochemical reaction in the body. Disorders result from a deficiency (or functional abnormality) of an enzyme. Archibald Garrod in 1902 was the first to attribute a disease to an enzyme defect: an inborn error of metabolism. Today, newborns are routinely screened for certain enzyme defects such as phenylketonuria (PKU) and galactosaemia, an error in the handling (metabolism) of the sugar galactose.
(12 Dec 1998)
defect, ventricular septal Hole in the interventricular septum, the wall between the ventricles (lower chambers of the heart). Commonly called a VSD. VSDs are a common class of heart deformity present at birth (congenital cardiac malformation).
(17 Dec 1998)
iodide transport defect See: familial goiter.
(05 Mar 2000)
iodotyrosine deiodinase defect See: familial goiter.
(05 Mar 2000)
oesophageal filling defect <radiology> Tumour, carcinoma (oesophagus, stomach extending proximally), leiomyoma / leiomyosarcoma, polyp: fibrovascular, inflammatory, adenomatous, papilloma, carcinosarcoma, lymphoma, metastasis, oesophageal varix, extrinsic lesion (vascular impression, adenopathy, cyst), foreign body
(12 Dec 1998)
osteoporotic marrow defect Focal osteoporotic bone marrow defect of the jaw; a focal radiolucent defect composed of normal marrow.
(05 Mar 2000)
Eisenmenger's defect The combination of ventricular septal defect with pulmonary hypertension and consequent right-to-left shunt through the defect, with or without an associated overriding aorta.
Synonym: Eisenmenger's defect, Eisenmenger's disease, Eisenmenger's tetralogy.
(05 Mar 2000)
endocardial cushion defect <radiology> Persistence of primitive atrioventricular canal and anomalies of AV valves associated with: Down syndrome: in 25% of Trisomy 21 an ECD is present; in 45% of ECD Trisomy 21 is present, asplenia/polysplenia types: complete (AV canal), partial findings: gooseneck deformity on angiogram, increased pulmonary vascularity, enlarged pulmonary artery, enlarged RV, LV, RA; normal LA (secondary to atrial septal defect)
(12 Dec 1998)
enzyme defect A disorder resulting from a deficiency (or functional abnormality) of an enzyme. In 1902 Archibald Garrod first attributed a disease to an enzyme defect: an inborn error of metabolism. Today, newborns are routinely screened for certain enzyme defects such as PKU (phenylketonuria) and galactosaemia, an error in the handling (metabolism) of the sugar galactose.
(12 Dec 1998)
fibrous cortical defect A common 1 to 3 cm defect in the cortex of a bone, most commonly the lower femoral shaft of a child, filled with fibrous tissue. Nonosteogenic or nonossifying fibroma by convention refers to lesions greater than 3 cm in diameter.
See: nonossifying fibroma.
Synonym: nonosteogenic fibroma.
(05 Mar 2000)
uterine filling defect <radiology> Technical, bubble, blood clot, mucoid material, congenital fold, pseudoadhesions / ridging -- folds long axis, neoplasm, submucosal leiomyoma, adenoma, endometrial carcinoma, pregnancy-related, pregnancy, molar pregnancy, retained conceptus, polyp, septated uterus, synechiae, IUD, iatrogenic (post-op)
(12 Dec 1998)
filling defect Displacement of contrast medium by a space-occupying lesion in a radiographic study of a contrast-filled hollow viscus, such as a polyp on a barium enema; also applied to defects in the otherwise uniform distribution of radionuclide in an organ, such as a metastasis in the liver on a 99mTc-sulfur colloid scan.
(05 Mar 2000)
filling defect in renal collecting system <radiology> Common causes: transitional cell carcinoma, blood clot, lucent calculus (urate) less common causes: fungus ball, sloughed papilla, fibroepithelial polyp, invasion by hypernephroma, malakoplakia, vessel impression, metastases
(12 Dec 1998)
lambdoid suture defect <radiology> Well-defined lucent lesion, classically unilateral, associated with neurofibromatosis
(12 Dec 1998)
luteal phase defect Inadequate function of the corpus luteum that may prevent a fertilized egg from implanting in the uterus or may lead to early pregnancy loss.
(09 Oct 1997)
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