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"lipoid proteinosis"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • lipid proteinosis
    ÁöÁú´Ü¹éÁõ
  • proteinosis
    ´Ü¹éÁõ
  • pulmonary alveolar proteinosis
    ÇãÆÄ²Ê¸®´Ü¹éÁõ, ÆóÆ÷´Ü¹éÁõ
  • lipoid
    1. ÁöÁú(¼º)- 2. À¯»çÁöÁú-
  • lipoid adrenal hyperplasia
    ÁöÁúºÎ½Å°ú´ÙÇü¼º
  • lipoid cell
    ÁöÁú¼¼Æ÷
  • lipoid infarct
    ÁöÁú°æ»ö
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  • ¿µ¹®
    ÇѱÛ
  • lipoid
    ÁöÁú¼º-
  • proteinosis
    ´Ü¹éÁõ
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  • ¿µ¹®
    ÇѱÛ
  • lipid proteinosis
    ÁöÁú´Ü¹éÁõ
  • proteinosis
    ´Ü¹éÁõ
  • pulmonary alveolar proteinosis
    Æó´Ü¹éÁõ, ÇãÆÄ²Ê¸®´Ü¹éÁõ
  • lipoid cell
    ÁöÁú¼¼Æ÷
  • lipoid adrenal hyperplasia
    ÁöÁúºÎ½Å°ú´ÙÇü¼º
  • lipoid infarct
    ÁöÁú¼º°æ»ö
  • lipoid
    ÁöÁú¼º-
  • lipoid nodule
    ÁöÁú¼º°áÀý
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  • alveolar proteinosis
    ÆóÆ÷¼º ´Ü¹éÁõ(¡­àõ Ó±ÛÜñø)
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø).
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø)
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø)
  • proteinosis, pulmonary alveolar
    ´Ü¹é(Áú)Áõ(Ó±ÛÜ(òõ)ñø), ÆóÆ÷¼º(øËøààõ)
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø).
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
  • pulmonary proteinosis
    ÆóÆ÷´Ü¹éÁõ.
  • pulmonary proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
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  • lipoid proteinosis
    À¯Áö¹æ¼º´Ü¹éÁõ
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  • alveolar proteinosis
    ÆóÆ÷¼º ´Ü¹éÁõ(¡­àõ Ó±ÛÜñø)
  • lipid proteinosis
    ÁöÁú´Ü¹éÁõ(¡­Ó±ÛÜñø).
  • nogenital alveolar proteinosis
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø).
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø)
  • proteinosis
    ´Ü¹éÁõ(Ó±ÛÜñø)
  • proteinosis, pulmonary alveolar
    ´Ü¹é(Áú)Áõ(Ó±ÛÜ(òõ)ñø), ÆóÆ÷¼º(øËøààõ)
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø).
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
  • pulmonary alveolar proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
  • pulmonary proteinosis
    ÆóÆ÷´Ü¹éÁõ.
  • pulmonary proteinosis
    ÆóÆ÷´Ü¹éÁõ(øËøàÓ±ÛÜñø)
  • familial lipoid degeneration
    °¡Á·¼º ÁöÁúº¯¼ºÁõ(Ê«ðéàõò·òõܨàõ
  • lipoid
    ¸®Æ÷À̵å, À¯ÁöÁú(×¾ò·òõ).
  • lipoid cell
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  • lipoid layer
    ÁöÁúÃþ
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  • lipoid
    ¸®Æ÷À̵å
  • proteinosis
    ´Ü¹éÁúÃàÀûÁõ(Ó±ÛÜòõõëîÝñø)
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  • pulmonary proteinosis
    ÆóÆ÷´Ü¹éÁõ
  • lipoid
    ¸®Æ÷À̵å, À¯ÁöÁú
  • lipoid pneumonia
    ¸®Æ÷À̵åÆó·Å, À¯ÁöÁúÆó·Å
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
CLAH congenital lipoid adrenal hyperplasia
LN Lesch-Nyhan [syndrome]; lipoid nephrosis; Lisch nodule; low necrosis; lupus nephritis; lymph node
PAP   1) Prostatic Acid Phosphatase; Àü¸³¼º »ê¼º ÀλêºÐÇØÈ¿¼Ò
  2) Primary Atypical Pneumoni...
ALP acute leukemia protocol; acute lupus pericarditis; alkaline phosphatase; alveolar proteinosis; anter...
PAP pancreatitis-associated protein; Papanicolaou [test]; papaverine; passive-aggressive personality; pa...
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lipoid CAH lipoid adrenal hyperplasia
PAP Pulmonary Alveolar Proteinosis
LN lipoid nephrosis
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    ¼³¸í
  • lipoid
    ¸®Æ÷À̵å, À¯ÁöÁú
    µ¿ÀǾî=adi
  • lipid proteinosis
    ÁöÁú ´Ü¹éÁõ
  • pulmonary alveolar proteinosis
    ÆóÆ÷ ´Ü¹éÁõ
    ÆóÆ÷ ³»¿¡ Æó °è¸éü ¼ººÐ°ú ºñ½ÁÇÑ ÀÎ ÁöÁúÀÌ ÃàÀûµÇ´Â ÁúȯÀÌ´Ù. ÀÌ ÁúȯÀº ÀÏÂ÷Àû
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
lipoid proteinosis <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness.
It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications.
inheritance: autosomal recessive.
Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 8 ÆäÀÌÁö: 1
alveolar proteinosis A very rare disease in which a phospholipid is widely distributed in cells and accumulates in the alveolar spaces in the lung. In some cases the underlying cause is unknown. In others it may relate to an infection or an immune system dysfunction. The net effect is a progressive interference in the ability of the lung (alveoli) to exchange oxygen and carbon dioxide.
Symptoms include cough, weight loss, fatigue, shortness of breath and nail abnormalities (clubbing). Chest X-ray may show infiltrates, but a bronchoscopy with trans-tracheal biopsy is necessary to make a tissue diagnosis or alveolar proteinosis. Spontaneous remission may occur in some individuals while complete respiratory failure occurs in others.
(27 Sep 1997)
proteinosis A state characterised by disordered protein formation and distribution, particularly as manifested by the deposition of abnormal proteins in tissues.
Origin: protein + G. -osis, condition
(05 Mar 2000)
pulmonary alveolar proteinosis <radiology> Overproduction of surfactant which can lead to alveolar (end-air-space) filling, peak age: 20 - 50 yrs, 33% asymptomatic, treatment: lavage Findings: bat-wing alveolar infiltrate, no interstitial disease, no adenopathy
(12 Dec 1998)
nephrosis, lipoid Glomerular disease causing heavy proteinuria characterised by absence of obvious histologic glomerular changes on light microscopy. It is also called minimal change glomerular disease and minimal lesion glomerulonephritis.
(12 Dec 1998)
lipoid 1. Resembling fat.
2. Former term for lipid.
Synonym: adipoid.
Origin: Lipo-+ G. Eidos, appearance
(05 Mar 2000)
lipoid granuloma Granuloma characterised by aggregates or accumulations of fairly large mononuclear phagocytes that contain lipid.
(05 Mar 2000)
lipoid nephrosis <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome in children affecting 2 to 3 children per 100,000 population under age 16 in the us. Minimal change disease is also seen rarely in adults.
The cause is unknown but may be related to an autoimmune illness. Risk factors include a history for a immune disorder, recent immunisation or a bee sting.
Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented.
(27 Sep 1997)
lipoid theory of narcosis That narcotic efficiency parallels the coefficient of partition between oil and water, and that lipoids in the cell and on the cell membrane absorb the drug because of this affinity.
Synonym: Meyer-Overton theory of narcosis.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Lipoid Proteinosis of Urbach and Wiethe - »õâ An autosomal recessive disorder characterized by glassy degenerative thickening (hyalinosis) of SKIN; MUCOSA; and certain VISCERA. This disorder is caused by mutation in the extracellular matrix protein 1 gene (ECM1). Clinical features include hoarseness and skin eruption due to widespread deposition of HYALIN.
    Synonyms : Lipoidproteinosis, Urbach-Wiethe Lipoid Proteinosis, Urbach-Wiethe Syndrome, Lipoid Proteinosis, Urbach-Wiethe, Urbach Wiethe Disease, Urbach Wiethe Lipoid Proteinosis
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