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  • ¿µ¹®
    ÇѱÛ
  • hyper-IgM syndrome
    °í¸é¿ª±Û·ÎºÒ¸°MÁõÈıº
  • hyperimmunoglobulin E syndrome
    °í¸é¿ª±Û·ÎºÒ¸°EÁõÈıº
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´Ùȯ±âÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
  • hypoventilation syndrome
    Àúȯ±âÁõÈıº
  • hemolytic uremic syndrome
    ¿ëÇ÷¿äµ¶ÁõÈıº
  • hemopleuropneumonic syndrome
    Ç÷¾×°¡½¿¸·Æó·ÅÁõÈıº, Ç÷¾×È丷Æó·ÅÁõÈıº
  • Hallervorden-Spatz syndrome
    ÇÒ·¯º¸¸£µ§-½´ÆÄÃ÷ÁõÈıº
  • hemorrhagic fever with renal syndrome
    ÃâÇ÷¿­ÄáÆÏÁõÈıº, ÃâÇ÷¿­½ÅÁõÈıº
  • hepatorenal syndrome
    °£ÄáÆÏÁõÈıº
  • hand-foot syndrome
    ¼Õ¹ßÁõÈıº
  • hantavirus pulmonary syndrome
    ÇÑŸ¹ÙÀÌ·¯½ºÆóÁõÈıº
  • Horner¡¯s syndrome
    È£³ÊÁõÈıº
  • Hunter¡¯s syndrome
    ÇåÅÍÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • fish-odor syndrome
    ¹°°í±âÇâÁõÈıº
  • floppy infant syndrome
    Àú±äÀ徯ÁõÈıº, ±äÀåÀúÇÏ¿µ¾ÆÁõÈıº
  • fragile X syndrome
    À¯¾à¿¢½ºÁõÈıº
  • gastrointestinal syndrome
    À§Àå°üÁõÈıº
  • general adaptation syndrome
    Àü½Å¼øÀÀÁõÈıº
  • green nail syndrome
    ³ì»ö¼Õ¹ßÅéÁõÈıº
  • hematopoietic syndrome
    Á¶Ç÷ÁõÈıº
  • hemolytic-uremic syndrome
    ¿ëÇ÷¿äµ¶ÁõÈıº
  • hemopleuropneumonic syndrome
    Ç÷¾×°¡½¿¸·ÇãÆÄÁõÈıº
  • hereditary adrenogenital syndrome
    À¯ÀüºÎ½Å¼º±âÁõÈıº
  • heredofamilial hypothalamohypophyseal syndrome
    À¯Àü°¡Á·½Ã»óÇϺγúÇϼöüÁõÈıº
  • hunger pain syndrome
    °øº¹ÅëÁõÈıº
  • hyperstimulation syndrome
    °ú´ÙÀÚ±ØÁõÈıº
  • hyperventilation syndrome
    °ú´ÙÈ£ÈíÁõÈıº
  • hyperviscosity syndrome
    °ú´ÙÁ¡¼ºÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Kallmann syndrome
    Ä®¸¸ÁõÈıº
  • Kanners syndrome
    Ä­³ÊÁõÈıº(~ñøý¦ÏØ)
  • Kassabach-Meritt syndrome
    Ä«»ç¹ÙÇÏ-¸Þ¸®Æ® ÁõÈıº
  • Kawasaki disease => mucocutaneous lymph node syndrome
    °¡¿Í»çŰ º´
  • Kernohan s syndrome
    Ä¿³ëÇÑÁõÈıº.
  • Kinky hair syndrome
    ŲŰÇì¾îÁõÈıº
  • Klinefelter s syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº.
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº
  • Klinefelters syndrome
    Ŭ¶óÀÎÆçÅÍÁõÈıº(¡­ñøý¦ÏØ)
  • Klippel Feli syndrome
    Ŭ¸®Æç-ÆäÀÏÁõÈıº.
  • Lambert-Eaton myasthenic syndrome
    ¶÷¹öÆ®-ÀÌÆ° ±Ù¹«·ÂÁõÁõÈıº
  • Landry Guillain Barre syndrome
    ¶õµå¸®-±æ·©-¹Ù·¹ÁõÈıº.
  • Laurence Moon Biedl syndrome
    ·Î·»½º-¹®-ºñµéÁõÈıº.
  • Lesch-Nyhan syndrome
    ·¹½¬ ´ÏÇÑ ÁõÈıº
  • Leser-Trelat syndrome
    ·¹Á¦¸£ Æ®·¼¶ó ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • sinus
    µ¿±¼
  • sinus [caverna]
    µ¿±¼
  • sinus anales ³ª
    Ç×¹®µ¿(ùýÚ¦÷Ó).
  • sinus aortae ³ª
    ´ëµ¿¸Æµ¿(ÓÞÔÑØæ÷Ó).
  • sinus arrest
    µ¿Á¤Áö(÷ÓïÎò­).
  • sinus arrest
    µ¿Á¤Áö(÷ÓïÎò­)
  • sinus arrhythmia
    µ¿ºÎÁ¤¸Æ(¡­ÝÕð¡Øæ), µ¿¼ººÎÁ¤¸Æ.
  • sinus arrhythmia
    µ¿ºÎÁ¤¸Æ(¡­ÝÕð¡Øæ), µ¿¼ººÎÁ¤¸Æ(Ô×àõÜôïÚØæ)
  • sinus barotrauma
    Ç×°øºÎºñ°­¿°(̰˭ËÓ Ë×˧Ëç).
  • sinus barotrauma
    Ç×°øºÎºñ°­¿°(ùþÍöÜùެ˷æú)
  • sinus block
    µ¿(¼º)ºí·Ï.
  • sinus block
    µ¿(¼º)ºí·Ï(Ô×àõ¡­)
  • sinus bradycardia
    µ¿¼­¸Æ(÷ÓßïØæ).
  • sinus bradycardia
    µ¿¼­¸Æ(÷ÓßïØæ)
  • sinus caroticus ³ª
    ¸ñµ¿¸Æµ¿, °æµ¿¸Æµ¿( ÔÑØæ÷Ó).
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CSN cardiac sympathetic nerve; carotid sinus nerve
CSNRT, cSNRT corrected sinus node recovery time
CSNS carotid sinus nerve stimulation
CSO claims services only; common source outbreak; craniostenosis; craniosynostosis; ostium of coronary s...
CSOP coronary sinus occlusion pressure
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AS Asperger Syndrome
AMS Atypical Mole syndrome
ALPS Autoimmune Lymphoproliferative Syndrome
APS I Autoimmune polyendocrine syndrome type I
APS-1 Autoimmune polyglandular syndrome type 1
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    ¼³¸í
  • clinical syndrome
    ÀÓ»ó ÁõÈıº, ÀÓ»óÀû ÁõÈıº
  • clumsy hand syndrome
    ¼­Å÷ ¼Õ ÁõÈıº
  • co-contraction syndrome
    µ¿½Ã ¼öÃà ÁõÈıº
  • Cockayne syndrome
    ÄÚÄÉÀÎ ÁõÈıº
  • Coffin-Lowry syndrome
    ÄÚÇÉ-·Î¸® ÁõÈıº
  • Cogan-Reese syndrome
    ÄÚ°£-¸®½º ÁõÈıº
  • congenital fibrosis syndrome
    ¼±Ãµ ¼¶À¯Áõ ÁõÈıº
  • congenital Q-T syndrome
    ¼±Ãµ¼º QT ÁõÈıº
  • congenital rubella syndrome
    ¼±Ãµ¼º dzÁø ÁõÈıº
    žư¡ ¸ðü ³»¿¡¼­ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î »ý±â´Â ÀÌ»ó Áõ¼¼. ÀӽŠÃʱâÀÇ ÀÓ»êºÎ°¡ dzÁø¿¡ °É¸®¸é žư¡ ¹ßÀ° Ãʱ⿡ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î Ãâ»ý ÈÄ¿¡ ´«ÀÇ ÀÌ»ó
  • conjunctivo-urethro-synovial syndrome
    °á¸· ´¢µµ Ȱ¸· ÁõÈıº
  • Conn syndrome
    ÄÜ ÁõÈıº
  • contiguous gene syndrome
    Á¢Ã˼º À¯ÀüÀÚ ÁõÈıº
  • cord compression syndrome
    ô¼ö ¾Ð¹Ú ÁõÈıº
  • corpus callosum syndrome
    ³ú·® ÁõÈıº
  • Cowden syndrome
    ÄÚ¿ìÅÙ ÁõÈıº
    ½Å»ý¹° ÁõÈıº. À¯µÎÁ¾°ú ºñ½ÁÇÑ º´¼Ò·Î ÀÚ°¥°°Àº ÇüÅÂÀÎ ¼¶µàÁ¾ÀÌ´Ù.
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uterine sinus A small irregular vascular channel in the endometrium, of a type that forms during pregnancy.
Synonym: uterine sinusoid.
Uteroplacental sinuses, irregular vascular spaces in the zone of the chorionic attachment to the decidua basalis.
(05 Mar 2000)
lactiferous sinus A circumscribed spindle-shaped dilation of the lactiferous duct just before it enters the nipple. In nursing mothers this dilatation stores a droplet of milk which is expressed by compression as the infant begins to suckle; this is thought to encourage continual suckling while the let-down reflex ensues.
Synonym: sinus lactiferi, ampulla lactifera, ampulla of milk duct, lactiferous ampulla.
(05 Mar 2000)
laryngeal sinus The recess in each lateral wall of the larynx between the vestibular and vocal folds and into which the layrngeal sacculus opens.
Synonym: ventriculus laryngis, laryngeal sinus, Morgagni's sinus, Morgagni's ventricle, sinus laryngeus.
(05 Mar 2000)
lateral sinus A paired dural venous sinus that drains the confluence of sinuses, running along the occipital attachment of the tentorium cerebelli and terminating in the sigmoid sinus.
Synonym: sinus transversus, lateral sinus.
Transverse pericardial sinus, a passage in the pericardial sac between the origins of the great vessels, i.e., posterior to the intrapericardial portions of the pulmonary trunk and ascending aorta and anterior to the superior vena cava and superior to the atria; it is formed as a result of the flexure of the heart tube, partially approximating the great venous and arterial vessels.
Synonym: sinus transversus pericardii, Theile's canal, transverse sinus of pericardium.
(05 Mar 2000)
frontal sinus One of the paired, but seldom symmetrical, air spaces located between the inner and outer compact layers of the frontal bone.
(12 Dec 1998)
frontal sinus aperture One of a pair of openings in the floor of the frontal sinuses in the nasal part of the frontal bone, through which the frontal sinuses communicate with the ethmoidal infundibulum via the frontonasal duct.
Synonym: apertura sinus frontalis.
(05 Mar 2000)
longitudinal sinus See: inferior sagittal sinus, superior sagittal sinus.
Longitudinal vertebral venous sinus, large, plexiform veins forming portions of the anterior internal vertebral venous plexus lying on the posterior surfaces of the vertebral bodies on either side of the posterior longitudinal ligament.
Synonym: sinus vertebrales longitudinales.
Luschka's sinus, venous sinus in the petrosquamous suture.
(05 Mar 2000)
lymphatic sinus The channels in a lymph node crossed by a reticulum of cells and fibres and bounded by littoral cells; there are subcapsular, trabecular, and medullary sinus's.
Synonym: lymph sinus.
Maier's sinus, an infundibuliform depression on the internal surface of the lacrimal sac which receives the lacrimal canaliculi.
Marginal sinuses of placenta, discontinuous venous lakes at the margin of the placenta.
(05 Mar 2000)
lymph sinus The channels in a lymph node crossed by a reticulum of cells and fibres and bounded by littoral cells; there are subcapsular, trabecular, and medullary sinus's.
Synonym: lymph sinus.
Maier's sinus, an infundibuliform depression on the internal surface of the lacrimal sac which receives the lacrimal canaliculi.
Marginal sinuses of placenta, discontinuous venous lakes at the margin of the placenta.
(05 Mar 2000)
Aarskog-Scott syndrome A syndrome of ocular hypertelorism, anteverted nostrils, broad upper lip, saddle-bag scrotum, and laxity of ligaments resulting in genu recurvatum, flat feet, and hyperextensible fingers; X-linked and autosomal dominant forms.
Synonym: Aarskog-Scott syndrome.
(05 Mar 2000)
Aarskog syndrome <syndrome> Grier et al. (1983) reported father and 2 sons with typical Aarskog syndrome, including short stature, hypertelorism, and shawl scrotum.
They tabulated the findings in 82 previous cases. X-linked recessive inheritance has been repeatedly suggested. The family reported by Welch (1974) had affected males in 3 consecutive generations. Thus, there is either genetic heterogeneity or this is an autosomal dominant with strong sex-influence and possibly ascertainment bias resulting from use of the shawl scrotum as a main criterion. Stretchable skin was present in the cases of Grier et al. (1983). Teebi et al. (1993) reported the case of an affected mother and 4 sons (including a pair of monozygotic twins) by 2 different husbands. They suggested that the manifestations were as severe in the mother as in the sons and that this suggested autosomal dominant inheritance. Actually, the mother seemed less severely affected, compatible with X-linked inheritance.
Clinical signs: Mild to moderate short stature,normocephaly, Widow's peak hair, maxillary hypoplasia, broad nasal bridge, anteverted nostrils, long philtrum, broad upper lip, curved linear dimple below the lower lip, hypertelorism, ptosis, down-slanted palpebral fissures, ophthalmoplegia, strabismus, hyperopic astigmatism, large cornea, floppy ears, lop-ears,cleft lip/palate, shawl scrotum, saddle-bag scrotum, cryptorchidism, brachydactyly, digital contractures, clinodactyly, mild syndactyly, transverse palmar crease, lymphoedema of the feet, ligamentous laxity, osteochondritis dissecans, proximal finger joint hyperextensibility, flexed distal finger joints, genu recurvatum, flat feet, stretchable skin, cervical spine hypermobility, odontoid anomaly, macrocytic anaemia, hemochromatosis, hepatomegaly, portal cirrhosis, imperforate anus, rectoperineal fistula, interstitial pulmonary disease, sternal deformity.
Inheritance: Sex-influenced autosomal dominant form, also X-linked form.
(05 Aug 1998)
abdominal muscle deficiency syndrome <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear.
(05 Mar 2000)
abstinence syndrome <syndrome> A constellation of physiologic changes undergone by persons or animals who have become physically dependent on a drug or chemical due to prolonged use at elevated doses, but who are abruptly deprived of that substance. The abstinence syndrome varies with the drug to which dependence has developed. Generally the effects observed are in an opposite direction from those produced by the drug; e.g., the withdrawal syndrome from central nervous system depressants such as barbiturates and benzodiazepines consists of insomnia, restlessness, tremulousness, hallucinations, and, in the extreme, tonic-clonic convulsions which may prove fatal. The onset time and severity of the abstinence syndrome depend upon how rapidly the drug disappears from the body.
(05 Mar 2000)
Achard syndrome <syndrome> Arachnodactyly with small receding mandible, broad skull, and joint laxity limited to the hands and feet; genetics unclear.
(05 Mar 2000)
Achard-Thiers syndrome <syndrome> One form of a virilizing disorder of adrenocortical origin in women, characterised by masculinization and menstrual disorders in association with manifestations of diabetes mellitus, such as glucosuria.
(05 Mar 2000)
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