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"congenital renal osteodystrophy"¿¡ ´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®
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  • renal collecting system
    ½ÅÁýÇÕ°ü°èÅë(ãìó¢ùêηͧ÷Ö).
  • renal collecting system
    ½ÅÁýÇÕ°ü°èÅë
  • renal column
    ½ÅÀå±âµÕ, ½ÅÁÖ(ãìñº).
  • renal column
    ÄáÆÏ±âµÕ
  • renal column of Bertin
    Bertin ½ÅÁÖ
  • renal columns
    ÄáÆÏ±âµÕ
  • renal columns ³ª columnae renales
    ½ÅÁÖ(ãìñº).
  • renal compensation
    ½Åº¸»ó.
  • renal compensation
    ½Å¼º´ë»ó(ãìàõÓÛßÁ).
  • renal contusion
    ½ÅÁ»ó
  • renal corpuscle
    ½ÅÀå¼Òü, ½Å¼Òü(ãìá³ô÷).
  • renal corpuscle
    ÄáÆÏ¼Òü
  • renal corpuscle
    ½Å¼Òü
  • renal cortex
    ÄáÆÏ°ÑÁú
  • renal cortical adenoma
    ½ÅÇÇÁú¼±Á¾
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  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • congenital immunologic thrombocytopenia
    ¼±Ãµ¼º ¸é¿ª¼º Ç÷¼ÒÆÇ°¨¼ÒÁõ(¡­Øóæ¹ àõúìá³÷ùÊõá´ñø).
  • congenital incontinence
    ¼±Ãµ¼º ½Ç±Ý(¡­ã÷Ð×).
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ.
  • congenital infection
    ¼±Ãµ°¨¿°
  • congenital intracranial tumor
    ¼±Ãµ¼º µÎ°³(°­)³»Á¾¾ç(¡­ÔéËÏË·Ò®ðþ åË).
  • congenital intussusception
    ¼±ÃµÃ¢ÀÚ°ãħÁõ
  • congenital laryngeal spasm
    ¼±Ãµ(¼º) Èĵο¬Ãà
  • congenital laryngeal stridor
    ¼±Ãµ(¼º) ÈĵÎõ¸í
  • congenital laryngeal web
    ¼±Ãµ(¼º) Èĵΰݸ·
  • congenital lip fistula
    ¼±Ãµ¼º ÀÔ¼ú ´©Ãâ°ü
  • congenital lipomatosis
    ¼±Ãµ¼º Áö¹æÁ¾Áõ
  • congenital lobar overinflation
    ¼±Ãµ¼º ´ë¿±°úµµÆØÃ¢(¡­ÓÞç¨Î¦Óøø³óì)
  • congenital localized absence of skin
    ¼±Ãµ¼º(à»ô¸àõ) ±¹¼Ò ÇǺΠ°á¼Õ
  • congenital lymphangiectatic edema
    ¼±Ãµ¼º ¸²ÇÁ°üÈ®ÀåºÎÁ¾(¡­Ý©ðþ).
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CEU congenital ectropion uveae; continuing education unit
CGFH congenital fibrous histiocytoma
CHB chronic hepatitis B; complete heart block; congenital heart block
CHBA congenital Heinz body hemolytic anemia
CHBHA congenital Heinz body hemolytic anemia
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CMD Congenital muscular dystrophies
CMD Congenital muscular dystrophy
CMT Congenital muscular torticollis
CMD Congenital myotonic dystrophy
CSNB Congenital stationary night blindness
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  • renal gout
    ½Å¼º Åëdz
  • renal hemangiopericytoma
    ½Å Ç÷°ü ÁÖÀ§ ¼¼Æ÷Á¾
  • renal hemophilia
    ½Å¼º Ç÷¿ìº´
  • renal hilus
    ½Å¹®
  • renal hypertension
    ½Å¼º °íÇ÷¾Ð
  • renal hypoplasia
    ½Å ¹ßÀ° ºÎÀü
  • renal impression
    ÄáÆÏ ÀÚ±¹
  • renal infantilism
    ½Å À¯¾ÆÁõ
  • renal injury
    ½Å ¼Õ»ó
  • renal ischemia
    ½Å ÇãÇ÷
  • renal lobe
    ÄáÆÏ ¿±
  • renal medulla
    ÄáÆÏ ¼ÓÁú
  • renal nanism
    ½Å¼º ³­ÀïÀÌ, ½Å¼º ³­ÀåÀÌÁõ
  • renal papillae
    ÄáÆÏ À¯µÎ
  • renal pedicle
    ½Å°æ
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toxoplasmosis, congenital Congenital infection with toxoplasma gondii characterised by lesions of the central nervous system.
(12 Dec 1998)
foot deformities, congenital Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth.
(12 Dec 1998)
limb deformities, congenital Congenital structural deformities of the upper and lower extremities collectively or unspecified.
(12 Dec 1998)
acute renal failure <nephrology> A sudden decline in renal function may be triggered by a number of acute disease processes.
Examples include sepsis (infection), shock, trauma, kidney stones, kidney infection, drug toxicity (aspirin or lithium), poisons or toxins (drug abuse) or after injection with an iodinated contrast dye (adverse effect).
Chronic renal failure represents a slow decline in kidney function over time. Chronic renal failure may be caused by a number of disorders which include long-standing hypertension, diabetes, congestive heart failure, lupus or sickle cell anaemia. Both forms of renal failure result in a life-threatening metabolic derangement.
(27 Sep 1997)
aminoaciduria, renal Impairment of renal tubular transport of amino acids.
(12 Dec 1998)
back-pressure renal atrophy <radiology> Caliectasis without obstruction, due to repeated episodes of obstruction, gradual loss of renal pyramids
(12 Dec 1998)
base of renal pyramid The outer broad part of a renal pyramid that lies next to the cortex.
Synonym: basis pyramidis renis.
(05 Mar 2000)
branchio-oto-renal syndrome <syndrome> An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to mondini type cochlear defect and stapes fixation.
(12 Dec 1998)
capsular branches of renal artery <anatomy, artery> Branches arising from the renal artery outside of the kidney that are distributed to the renal capsule.
Synonym: rami capsulares arteriae renalis.
(05 Mar 2000)
captopril renal scan <radiology> In a kidney with a lesion in the afferent arteriole (e.g. Atherosclerotic plaque), reflex constriction of the efferent arteriole occurs through angiotensin system thus maintaining renal perfusion. ACE inhibition prevents constriction of efferent arteriole. Therefore, perfusion is decreased to a kidney with afferent lesions and the renal scan to looks WORSE. Bottom line: renal scans appear WORSE with captopril administration if there is a lesion in the afferent arteriole. See: renal artery stenosis
(12 Dec 1998)
carcinoma, renal cell Carcinoma of the renal parenchyma usually occurring in middle age or later and composed of tubular cells in varying arrangements. It was first described in 1826. Possible causal factors are environmental, hormonal, cellular, and genetic. Smoking is a definite risk factor and obesity is associated with increased risk. Renal cell carcinoma accounts for approximately 3% of adult cancer; the male-female ratio is 2:1. It is more common among urban residents than rural.
(12 Dec 1998)
renal <anatomy> Pertaining to the kidney, nephric.
(18 Nov 1997)
renal adenocarcinoma <radiology> Hypernephroma, renal cell carcinoma, arises from proximal collecting tubule, 10% bilateral adenocarcinoma types: papillary, alveolar, onchocytoma vascularity, 85% hypervascular (require pre-op embolization), 10% hypovascular (usually papillary type), 5% avascular associated with: tuberous sclerosis, von Hippel-Lindau syndrome see also: staging
(12 Dec 1998)
renal adenocarcinoma: staging <radiology> Typical presentation: Haematuria . . . . . 70% Fever . . . . . . . 16% Pain . . . . . . . . 50% Polycythemia . . . . 3% Palpable mass . . . 20% Anatomic staging (TNM): T1 Small tumour, kidney not enlarged T2 Large tumour, contained within renal capsule T3 Extension into perinephric fat or renal vein T4 Invasion of adjacent organs
(12 Dec 1998)
renal adenocarcinoma: vascularity <radiology> 85% hypervascular (require pre-op embolization), 10% hypovascular (usually the papillary type), 5% avascular also: 10% are bilateral
(12 Dec 1998)
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