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"Polycystic Kidney, Autosomal Recessive"¿¡ ´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
  • homozygous recessive
    µ¿Á¾Á¢ÇÕ¿­¼º-
  • recessive
    1. ¿­¼º- 2. ¿­¼º¼ÒÁú, ¿­¼º´ë¸³À¯ÀüÀÚ
  • recessive character
    ¿­¼ºÇüÁú
  • recessive gene
    ¿­¼ºÀ¯ÀüÀÚ
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • recessive heredity
    ¿­¼ºÀ¯Àü
  • recessive inheritance
    ¿­¼ºÀ¯Àü
  • recessive mutation
    ¿­¼ºµ¹¿¬º¯ÀÌ
  • recessive trait
    ¿­¼º¼ÒÁú
  • X-linked recessive inheritance
    X¿¬°ü¿­¼ºÀ¯Àü
  • arteriosclerotic kidney
    µ¿¸Æ°æÈ­ÄáÆÏ, µ¿¸Æ°æÈ­½ÅÀå
  • artificial kidney
    ÀΰøÄáÆÏ, Àΰø½ÅÀå
  • atrophic kidney
    À§ÃàÄáÆÏ, À§Ãà½ÅÀå
  • acquired cystic kidney disease
    ÈÄõ³¶¼ºÄáÆÏº´, ÈÄõ³¶¼º½ÅÀ庴
  • amyloid kidney
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏ, ¾Æ¹Ð·ÎÀ̵å½ÅÀå
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  • ¿µ¹®
    ÇѱÛ
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • recessive gene
    ¿­¼ºÀ¯ÀüÀÚ
  • homozygous recessive
    µ¿Á¾Á¢ÇÕ¿­¼º
  • recessive heredity
    ¿­¼ºÀ¯Àü
  • recessive homozygote
    ¿­¼ºÈ£¸ðÁ¢ÇÕü
  • recessive inheritance
    ¿­¼ºÀ¯Àü
  • X-linked recessive inheritance
    ¿¢½º¿¬°ü¿­¼ºÀ¯Àü
  • recessive mutation
    ¿­¼ºµ¹¿¬º¯ÀÌ
  • recessive dystrophic epidermolysis bullosa
    ¿­¼ºÀ§Ã๰ÁýÇ¥Çǹڸ®Áõ
  • recessive
    ¿­¼º
  • recessive trait
    ¿­¼º¼ÒÁú
  • acquired cystic kidney disease
    ÈÄõ³¶¼ºÄáÆÏº´
  • amyloid kidney
    ¾Æ¹Ð·ÎÀ̵åÄáÆÏ, ¾Æ¹Ð·ÎÀ̵å½ÅÀå
  • arteriosclerotic kidney
    µ¿¸Æ°æÈ­ÄáÆÏ
  • artificial kidney
    ÀΰøÄáÆÏ
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    ÇѱÛ
  • recessive
    ¿­¼º(æëàõ)
  • recessive
    ¿­¼º(æëàõ)ÀÇ
  • recessive
    ¿­¼ºÇüÁú.
  • recessive
    ¿­¼ºÀÇ.
  • recessive character
    ¿­¼ºÇüÁú(¡­û¡òõ).
  • recessive dystrophic epidermolysis bullosa
    ¿­¼º ¿µ¾çÀå¾Ö ¼öÆ÷ Ç¥Çǹڸ®Áõ
  • recessive gene
    ¿­¼ºÀ¯ÀüÀÚ(¡­ë¶îîí­).
  • recessive gene
    ¿­¼ºÀ¯ÀüÀÚ
  • recessive gonosomal gene
    ¿­¼º¼º¿°»öüÀ¯ÀüÀÚ
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´(¡­ë¶îîÜ»).
  • recessive heredity
    ¿­¼ºÀ¯Àü(¡­ë¶îî).
  • recessive homozygote
    ¿­¼ºÈ£¸ðÁ¢ÇÕü(¡­ïÈùêô÷).
  • recessive inheritance
    ¿­¼ºÀ¯Àü(¡­ë¶îî).
  • recessive lethals
    ¿­¼ºÄ¡»çÀÎ(¡­öÈÞÝì×).
  • recessive mutation
    ¿­¼ºµ¹¿¬º¯ÀÌ(æëàõÔÍæÔܨì¶).
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  • ¿µ¹®
    ÇѱÛ
  • polycystic disease
    ´Ù³¶¼º Áúȯ(ÒýÒ¥àõ òðü´)
  • polycystic lung
    ¹µ¹°È¤ÇãÆÄ
  • polycystic ovarian disease
    ´Ù³¶³­¼Ò(ÒýÒ¥Õ°áµ), ´Ù³¶¼º ³­¼Òº´(ÒýÒ¥àõ Õ°áµÜ»)
  • polycystic ovarian syndrome
    ´Ù³¶¼º ³­¼ÒÁõÈıº.
  • polycystic ovary
    ´Ù³¶³­¼Ò(¡­Õ°áµ).
  • polycystic ovary
    ´Ù³¶³­¼Ò(ÒýÒ¥Õ°áµ)
  • autosomal
    »ó¿°»öü¼º(ßÈæøßäô÷àõ)
  • autosomal
    »ó¿°»öü(ÀÇ).
  • autosomal abnormality
    »ó¿°»öüÀÌ»ó(¡­æøßäô÷ì¶ßÈ).
  • autosomal dominant
    »ó¿°»öü ¿ì¼º
  • autosomal dominant disorder
    »ó¿°»öü¿ì¼º À¯ÀüÁúȯ.
  • autosomal dominant disorders
    »ó¿°»öü ¿ì¼ºÁúȯ(ßÓæøßäô÷éÐàõòðü´)
  • autosomal dominant inheritance
    »ó¿°»öü¿ì¼ºÀ¯Àü(¡­éÐàõë¶îî).
  • autosomal dominant trait
    »ó¿°»öü¿ì¼ºÀ¯ÀüÇüÁú.
  • autosomal gene
    º¸Åë¿°»öüÀ¯ÀüÀÚ
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    ÇѱÛ
  • kidney, atrophic
    À§Ãà½Å
  • kidney, contracted
    À§Ãà½Å
  • kidney, horseshoe
    ¸¶Á¦Ã¶½Å
  • kidney, rudimentary
    ÈçÀû½Å
  • KUB [=kidney, ureter and bladder]
    ½Å-´¢°ü-¹æ±¤ ´Ü¼øÃÔ¿µ
  • medullary sponge kidney
    ¼öÁú¼ºÇظé(»ó)½Å
  • movable kidney
    À̵¿½Å, À¯ÁÖ½Å
  • percutaneous needle biopsy of kidney
    °æÇǽÅħ»ý°Ë
  • solitary kidney
    ´Ü½Å(Áõ)
  • sponge kidney
    ÇØ¸é½Å
  • trifid kidney
    »ï¿­½Å
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
AROA autosomal recessive ocular albinism
ARSACS autosomal recessive spastic ataxia of Charlevoix-Saguenay
PHAVER pterygia-heart defects-autosomal recessive inheritance-vertebral defects-ear anomalies-radial defect...
PKD polycystic kidney disease; proliferative kidney disease
APCD acquired prothrombin complex deficiency [syndrome]; adult polycystic kidney disease
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
SCARMD Severe childhood autosomal recessive muscular dystrophy
APKD Adult polycystic kidney disease
PKD Polycystic kidney disease
PKD1 Polycystic kidney disease 1
RXLI Recessive X-linked ichthyosis
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    ¼³¸í
  • autosomal inheritance
    »ó¿°»öü¼º À¯Àü
  • autosomal trisomy
    »ó¿°»öü »ïü¼º
  • pedigree pattern of autosomal dominant trait
    »ó¿°»öü¼º ¿ì¼º ÇüÁúÀÇ °¡°èµµ
  • cadaver kidney
    »çü ½Å, »çü ½ÅÀå
  • cake kidney
    ¿ÏÀü À¶ÇÕ ½Å
  • cicatricial kidney
    ¹ÝÈç½Å
    È­³ó¼º ½Å¿ì½Å¿°¿¡¼­ »ý±â´Â À§ÃàµÈ ¹ÝÈ缺 ½ÅÀå.
  • cystic kidney
    ³¶½Å
  • double kidney
    Áߺ¹ ½Å
  • duplex kidney
    Áߺ¹ ½Å
  • dysplastic kidney
    ½Å ÀÌÇü¼º
  • embryoma of kidney
    ½Å ¹è¾ÆÁ¾
  • fibrous capsule of kidney
    ½Ã ¼¶À¯ ÇǸ·
  • hemangioma of kidney
    ½Å Ç÷°üÁ¾
  • hypoplastic kidney
    ¹ßÀ° ºÎÀü ½Å
  • kidney donor
    ½Å Á¦°øÀÚ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
recessive inheritance dominance of traits
recessive oncogene <molecular biology> A single copy of this gene issufficient to suppress cell proliferation, the loss of both copies of the gene contributes to cancer formation.
(09 Oct 1997)
recessive trait See: dominance of traits.
(05 Mar 2000)
recessive, x-linked A gene on the X chromosome that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, duchenne muscular dystrophy (dmd) is an x-linked recessive disorder. A dmd boy has the dmd gene on his sole x chromosome (and so is said to be hemizgous for dmd). Although it is much rarer, a girl can have dmd (by several different means as, for example, if she has the dmd gene on both her x chromosomes and so is homozygous for dmd).
(12 Dec 1998)
polycystic Composed of many cysts.
(05 Mar 2000)
polycystic disease of kidneys A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance.
Synonym: polycystic disease of kidneys.
(05 Mar 2000)
polycystic liver Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs.
Synonym: polycystic liver disease.
(05 Mar 2000)
polycystic liver disease Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs.
Synonym: polycystic liver disease.
(05 Mar 2000)
polycystic ovarian disease <disease> A condition found among women who do not ovulate, characterised by multiple ovarian cysts and increased androgen production.
(09 Oct 1997)
polycystic ovary Enlarged cystic ovary's, pearl white in colour, with thickened tunica albuginea, characteristic of the Stein-Leventhal syndrome; clinical features are abnormal menses, obesity, and evidence of masculinization, such as hirsutism.
(05 Mar 2000)
polycystic ovary syndrome <syndrome> Clinical symptom complex characterised by oligomenorrhoea or amenorrhoea, anovulation, and regularly associated with bilateral polycystic ovaries.
(12 Dec 1998)
disease, ovarian, polycystic See Disease, polycystic ovarian.
(12 Dec 1998)
disease, polycystic ovarian An hormonal problem that causes women to have a variety of symptoms including irregular or no periods, acne, obesity and excessive hair growth. Women with PCO are at a higher risk for uterine cancer (endometrial cancer), diabetes, high blood pressure, and heart disease. With proper treatment, risks can be minimised. PCO is also known as Stein-Leventhal syndrome.
(12 Dec 1998)
acute kidney 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)
acute kidney transplant rejection <radiology> Findings on ultrasound: globular enlargment of the kidney, swelling and hypoechogenicity of the medullary pyramids, indistinct cortico-medullary junction, foci in the renal cortex
(12 Dec 1998)
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