| ¿µ¹® | cervical vertebra | ÇÑ±Û | ¸ñ»À, °æÃß |
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| ¼³¸í | ôÃß Áß¿¡¼ ¸ñºÎºÐÀ» ÀÌ·ç´Â ôÃß»À¸¦ À̸£´Â ¸»ÀÌ´Ù. ôÁÖÀÇ ½ÃÀÛÀΠù¹øÂ° ôÃß»À¿¡¼ºÎÅÍ 7¹øÂ° ôÃß»À±îÁö¸¦ ¸»ÇÑ´Ù. ¸ñÀÖ´Â Æú¸³(sessile polyp) ±â½ÃºÎ°¡ ³ÐÀº ¸ð¾çÀ» °¡Áö°í ³»°³»·Î µ¹ÃâµÇ¾î ³ª¿Â Æú¸³À» ¸»ÇÑ´Ù. ÀÌ¿¡ ºñÇØ Á¼Àº Áٱ⿡ ÀÇÇØ ÁöÅʵǴ Æú¸³À» ¸ñÀÖ´Â Æú¸³À̶ó ÇÑ´Ù. |
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| ¿µ¹® | fibrous dysplasia | ÇÑ±Û | ¼¶À¯Çü¼ºÀÌ»ó |
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| ¼³¸í | ±¹¼Ò ¹ßÀ°Àå¾Ö·Î »ÀÀÇ ¸ðµç ¼ººÐÀÌ ³ªÅ¸³ª³ª ¼º¼÷ÇÑ ±¸Á¶·Î ºÐÈÇÏÁö´Â ¸øÇÏ´Â º´ÀÌ´Ù. ÀÓ»óÀ¸·Î ÇϳªÀÇ »À ȤÀº ¿©·¯°³ÀÇ »À¸¦ µ¿½Ã¿¡ ħ¹üÇÒ ¼ö ÀÖ´Ù. ¿©·¯»À À¯ÇüÀº °¥»ö»ö¼Ò Ä§Âø°ú ³»ºÐºñ Àå¾Ö¸¦ µ¿¹ÝÇϸç Á¶¼÷ÇÑ ¼ºÀû ¹ßÀ°À» µ¿¹ÝÇÑ´Ù. À°¾È¼Ò°ßÀ¸·Î °æ°è°¡ ¶Ñ·ÇÇÑ º´ÅÍ·Î Á¶Á÷¼Ò°ßÀ¸·Î´Â ¼¶À¯¸ð¼¼Æ÷ÀÇ Áõ½Ä°ú °î¼±»óÀÇ »ÀÀܱâµÕÀ¸·Î ±¸¼ºµÇ¾î Àִµ¥ »ÀÀܱâµÕÀº »À¸ð¼¼Æ÷·Î µ¤¿©ÀÖÁö ¾ÊÀº ¹«Ãþ»À(woven bone)ÀÌ´Ù. |
||
| C. | 1) Candida C. Albicans C. Guillier... |
|---|---|
| HIVD | Herniation(Herniated) of Inter-Vertebral Disc - Cervical HIVD &... |
| C1 | first cervical nerve; first cervical vertebra; first component of complement |
| C2 | second cervical nerve; second cervical vertebra; second component of complement |
| C3 | third cervical nerve; third cervical vertebra; third component of complement |
| CIN | Cervical Intraephithelial Neoplasia |
|---|---|
| CIN 3 | Cervical Intraepithelial Neoplasia grade 3 |
| CC | Cervical cancer |
| CC | Cervical carcinoma |
| CD | Cervical dystonia |
| cervical dysplasia | A term which describes precancerous changes to the epithelial cells lining the cervix. The diagnosis is made from the microscopic examination of a PAP smear acquired tissue specimen. Less than 5% of all PAP smears will show cervical dysplasia. The peak incidence is in women 25 to 35 years of age. Risk factors include multiple sexual partners, early onset of sexual activity (less than 18), early childbearing (less than 16) and past medical history of a sexually transmitted disease (for example genital warts, genital herpes, HIV infection). Treatment is based on the degree of dysplasia present, as judged by a pathologist. Treatments include cryotherapy and conisation. Origin: Gr. Plassein = to form (27 Sep 1997) |
|---|
| anhidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
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| anterofacial dysplasia | Abnormal growth of the face or cranium in an anteroposterior direction as seen and measured with a cephalogram. (05 Mar 2000) |
| arrhythmogenic right ventricular dysplasia | A congenital cardiomyopathy in which transmural infiltration of adipose tissue results in weakness and aneurysmal bulging of the infundibulum, apex, and posterior basilar region of the right ventricle and leads to ventricular tachycardia arising in the right ventricle. (12 Dec 1998) |
| asphyxiating thoracic dysplasia | Hereditary hypoplasia of the thorax, associated with pelvic skeletal abnormality. Synonym: asphyxiating thoracic chondrodystrophy, Jeune's syndrome, thoracic-pelvic-phalangeal dystrophy. (05 Mar 2000) |
| bronchopulmonary dysplasia | <embryology, paediatrics> A form of chronic lung disease of uncertain cause sometimes seen in children who have received mechanical respiratory support (with high oxygenation) in the neonatal period. Often associated with those infants who have been treated for hyaline membrane disease. Origin: Gr. Plassein = to form (27 Sep 1997) |
| mammary dysplasia | An obsolete term for fibrocystic condition of the breast. (05 Mar 2000) |
| mandibulofacial dysplasia | A hereditary disorder occurring in two forms: the complete form (franceschetti's syndrome) is characterised by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (treacher collins syndrome) is characterised by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (12 Dec 1998) |
| ventriculoradial dysplasia | A congenital syndrome consisting of a ventricular septal defect with associated absence of thumb or radius. (05 Mar 2000) |
| cerebral dysplasia | Abnormal development of the telencephalon. (05 Mar 2000) |
| retinal dysplasia | <ophthalmology> Congenital, often bilateral, retinal abnormality characterised by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. (12 Dec 1998) |
| cervix dysplasia | A spectrum of histologic changes in the epithelium of the cervix uteri which may begin as a superficial lesion and progress to invasive carcinoma. (12 Dec 1998) |
| periapical cemental dysplasia | <dentistry> A benign, painless, non-neoplastic condition of the jaws which occurs almost exclusively in middle-aged black females. The lesions are usually multiple, most frequently involve vital mandibular anterior teeth, surround the root apices, and are initially radiolucent (becoming more opaque as they mature). Synonym: periapical osteofibrosis. (21 Jun 2000) |
| metaphyseal dysplasia | <radiology> (Pyle disease) also known as: craniometaphyseal dysplasia, autosomal recessive, failure of modeling of cylindrical bones, Erlenmeyer flask appearance of metaepiphyses (12 Dec 1998) |
| metaphysial dysplasia | An abnormality that occurs when new bone at the metaphyses of long bones fails to undergo remodeling to the normal tubular structure; the ends of long bones appear to be expanded and porotic, with thin cortex; there may be an associated overgrowth of cranial bones (craniometaphysial dysplasia). (05 Mar 2000) |
| chondroectodermal dysplasia | Triad of chondrodysplasia, ectodermal dysplasia, and polydactyly, with congenital heart defects in over half of patients; autosomal recessive inheritance. Synonym: Ellis-van Creveld syndrome. (05 Mar 2000) |
| cervical dysplasia |
Cervical dysplasia refers to a medical condition of the cervix in which squamous cells on the surface of the cervix undergo a premalignant transformation. This abnormal growth (dysplasia) may lead to the development of cervical cancer if left untreated. Cervical dysplasia can be diagnosed by a biopsy of the cervix. An abnormal Pap smear may lead to a recommendation for colposcopy of the cervix during which the cervix is examined under magnification. ...
Ãâó: en.wikipedia.org/wiki/Cervical_dysplasia
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|---|---|
| cervical dysplasia |
Abnormality in the size, shape, and organization of adult cells of the cervix. Often a precursor lesion for cervical cancer. Studies indicate an increase in prevalence of cervical dysplasia among women living with HIV. Additional studies have documented that a higher prevalence is associated with greater immune suppression. HIV infection may also adversely affect the clinical course and treatment of cervical dysplasia and cancer.
Ãâó: www.amfar.org/cgi-bin/iowa/bridge.html
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| cervical dysplasia |
Abnormal cells from the cervix that may indicate a pre-cancerous condition.
Ãâó: www.thebody.com/hivnews/aidscare/dec97/pullout.htm...
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| cervical dysplasia |
abnormal changes (eg, in size, shape, growth pattern) of the cells of the uterine cervix, which may be detected by a Pap smear or colposcopy. Cervical dysplasia is associated with the human papillomavirus (HPV) and may progress to cervical cancer.
Ãâó: www.sfaf.org/treatment/beta/b38/b38glos.html
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| cervical dysplasia |
A disease of the membrane that covers the cervix. It is often considered to be pre-cancerous and should be treated.
Ãâó: www.sexualcounselling.com/Glossary/Glossaryc.htm
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