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  • ¿µ¹®
    ÇѱÛ
  • 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
  • visual defect
    ½Ã(°¢)°á¼Õ
  • visual field defect
    ½Ã¾ß°á¼Õ
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    ÇѱÛ
  • 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
  • sensory defect
    °¨°¢°á¼Õ
  • separation defect
    ºÐ¸®°áÇÔ
  • septal defect
    »çÀ̸·°á¼Õ, Á߰ݰá¼Õ
  • septation defect
    »çÀ̸·Çü¼º°áÇÔ
  • skull bone defect
    ¸Ó¸®»À°á¼Õ, µÎ°³°ñ°á¼Õ
  • synthesis defect
    ÇÕ¼º°áÇÔ
  • transport defect
    ¿î¹Ý°áÇÔ
  • ventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • visual defect
    ½Ã°¢°á¼Õ
  • visual field defect
    ½Ã¾ß°á¼Õ
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  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè).
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè)
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  • auditory defect
    û°á¼Õ
  • basic defect
    ±âº»Àû °á¼Õ
  • canalisation defect
    °üÇü¼º°áÇÔ
  • cerebral defect syndrome
    ³úÀå¾ÖÁõÈıº(Òàî¡äôñøý¦ÏØ).
  • chromosomal defect
    ¿°»öü°áÇÔ
  • chromosomal defect
    ¿°»öü °á¼Õ(æøßäô÷ÌÀáß)
  • cleavage defect
    ºÐÇÒ°áÇÔ
  • combined ventilatory defect
    º¹ÇÕ¼ºÈ¯±âÀå¾Ö
  • common atrioventricular canal defect
    °øÅë¹æ½Ç°ü°á¼Õ(Áõ).
  • common atrioventricular canal defect
    °øÅë¹æ½Ç°ü°á¼Õ(Áõ).
  • composition defect
    ±¸¼º°áÇÔ
  • conduction defect
    ÀüµµÀå¾Ö(¡­î¡äô).
  • congenital color vision defect
    ¼±Ãµ»ö°¢ÀÌ»ó
  • congenital defect
    ¼±Ãµ¼º °á¼Õ(Áõ)(¡­ÌÀáßñø).
  • congenital defect
    ¼±Ãµ°áÇÔ
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  • Amniotic defect
    ¾ç¸·°áÇÔ
    [¿¾ ¿ë¾î] ¾ç¸·°áÇÔ
  • Facial defect
    ¾ó±¼°áÇÔ
    [¿¾ ¿ë¾î] ¾È¸é°áÇÔ
  • Chromosomal defect
    ¿°»öü°áÇÔ
    [¿¾ ¿ë¾î] ¿°»öü°áÇÔ
  • Heritable defect
    À¯Àü°áÇÔ
    [¿¾ ¿ë¾î] À¯Àü¼º°áÇÔ
  • Fusion defect
    À¶ÇÕ°áÇÔ
    [¿¾ ¿ë¾î] À¶ÇÕ°áÇÔ
  • Fusion defect (Cleft palate)
    À¶ÇÕ°áÇÔ (ÀÔõÀå°¥¸²Áõ)
    [¿¾ ¿ë¾î] À¶ÇÕ°áÇÔ (ÀÔõÀå°¥¸²Áõ)
  • Aggregation defect
    ÀÀÁý°áÇÔ
    [¿¾ ¿ë¾î] ÀÀÁý¼º°áÇÔ
  • Migration defect
    ÀÌÁÖ°áÇÔ
    [¿¾ ¿ë¾î] ÀÌÁÖ°áÇÔ
  • Defect of palate
    ÀÔõÀå°áÇÔ
    [¿¾ ¿ë¾î] ±¸°³°áÇÔ
  • Total heart defect
    Àüü½ÉÀå°áÇÔ
    [¿¾ ¿ë¾î] ½ÉÀåÀü°áÇÔ
  • Plication defect
    ÁÖ¸§Çü¼º°áÇÔ
    [¿¾ ¿ë¾î] ÁÖ¸§Çü¼º°áÇÔ
  • Plication defect (Schistomyelia)
    ÁÖ¸§Çü¼º°áÇÔ (ô¼ö°¥¸²Áõ)
    [¿¾ ¿ë¾î] ÁÖ¸§Çü¼º°áÇÔ (ô¼ö°¥¸²Áõ)
  • Defect of implantation
    Âø»ó°áÇÔ
    [¿¾ ¿ë¾î] Âø»ó°áÇÔ
  • Defect of spinal cord
    ô¼ö°áÇÔ
    [¿¾ ¿ë¾î] ô¼ö°áÇÔ
  • Defect of vertebral column
    ôÁÖ°áÇÔ
    [¿¾ ¿ë¾î] ôÁÖ°áÇÔ
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CVB chorionic villi biopsy
CVS cardiovascular surgery; cardiovascular system; challenge virus strain; chorionic villi sampling; cle...
hCFSH human chorionic follicle-stimulating hormone
HCG, hCG human chorionic gonadotropin
HCS Hajdu-Cheney syndrome; Hazard Communication Standard; health care support; hourglass contraction of ...
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hCG Beta-human chorionic gonadotropin
CG Chorionic Gonadotropin
CVS Chorionic Villi Sampling
CVS Chorionic Villus Samples
CVS Chorionic Villus Sampling
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
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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