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"lamellar ichthyosis"¿¡ ´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
  • ichthyosis vulgaris ³ª
    ½É»ó¼º ¾î¸°¼±(ãüßÒàõåàìçàÈ)
  • ichthyosis ³ª
    ¾î¸°¼±(åàìçàÈ)
  • plaques lisses =leukoplakia, ichthyosis linguae
    ÆòȰ¹Ý(øÁüÁÚè).
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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  • lamellar keratoplasty
    Ç¥Ãþ°¢¸·À̽Ä(¼ú)(öµßÒÊÇØ¯ì¹ãÕâú).
  • lamellar macular hole
    Ç¥ÃþȲ¹Ý¿ø°ø
  • lamellar membranous bone secondary membranous bone
    ÃþÆÇ¸·»À ÀÌÂ÷¸·»À
  • lamellar membranous boneÃþÆÇ¸·
    lamellar membranous boneÃþÆÇ¸·
  • lamellar process
    ÆÇµ¹±â
  • lamellar resection
    ÃþÆÇÀýÁ¦(¼ú)
  • lamellar retinal hole
    Ç¥Ãþ¸Á¸·¿­°ø
  • lamellar sheath =perineurium
    Ãþ»óÃÊ(öµßÒôú).
  • acquired ichthyosis
    ÈÄõ¼º(ý­ô¸àõ)¾î¸°¼±(åà×÷àÈ)
  • autosomal recessive ichthyosis
    »ó¿°»öü¿­¼º¾î¸°¼±
  • congenital ichthyosis
    ¼±Ãµ(¼º) ¾î¸°¼±(¡­åàìçàÈ).
  • congenital ichthyosis
    ¼±Ãµ¼º(à»ô¸àõ)¾î¸°¼±(åà×÷àÈ)
  • epidermal dysplasia (ichthyosis)
    Ç¥ÇÇÇü¼ºÀå¾Ö (ºñ´Ã¹öÁò)
  • fetal ichthyosis
    žƾ¼±(¡­åàìçàÈ).
  • harlequin ichthyosis
    ¹ìÇǺξ¼±
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
IBIDS ichthyosis-brittle hair-impaired intelligence-decreased fertility-short stature [syndrome]
ICE ice, compression, elevation; ichthyosis-cheek-eyebrow [syndrome]; immunochemical evaluation; interle...
IFAP ichthyosis follicularis-atrichia-photophobia [syndrome]
IHCM ichthyosis hystrix, Curth-Macklin [type]
ILC ichthyosis linearis circumflex; incipient lethal concentration
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XLI X-Linked ichthyosis
LB's lamellar bodies
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 13 ÆäÀÌÁö: 2
ichthyosis follicularis A form of autosomal dominant type of ichthyosis, with horny follicular plugging of the extensor surfaces of the extremities; onset in early childhood.
(05 Mar 2000)
ichthyosis hystrix See: bullous congenital ichthyosiform erythroderma
Origin: G. Hystrix, hedgehog
(05 Mar 2000)
ichthyosis intrauterina most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
(12 Dec 1998)
ichthyosis linearis circumflexa Congenital or infantile migratory polycyclic erythema and scaling that shows a peripheral double margin; persists throughout life and may be associated with trichorrhexis invaginata in Netherton's syndrome; autosomal recessive inheritance.
(05 Mar 2000)
ichthyosis palmaris et plantaris The occurrence of symmetrical diffuse or patchy areas of hypertrophy of the horny layer of the epidermis on the palms and soles; a group of ectodermal dysplasias of considerable variety, and either autosomal dominant or recessive inheritance.
Synonym: ichthyosis palmaris et plantaris, keratoderma palmaris et plantaris, keratoderma symmetrica, keratoma plantare sulcatum, keratosis palmaris et plantaris, tylosis palmaris et plantaris.
(05 Mar 2000)
ichthyosis scutulata Ichthyosis marked by diamond-shaped or shield-shaped lesions.
(05 Mar 2000)
ichthyosis sebacea The presence of an unusual amount of vernix caseosa.
(05 Mar 2000)
ichthyosis sebacea cornea A type of ichthyosis with vernix caseosa as seen in the newborn.
(05 Mar 2000)
ichthyosis simplex most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
(12 Dec 1998)
ichthyosis spinosa A genodermatosis characterised by diffuse chronic erythema and scale formation which may be separated into bullous and nonbullous forms.
Synonym: ichthyosiform erythroderma, ichthyosis spinosa, keratoma malignum.
(05 Mar 2000)
ichthyosis uteri Transformation of the columnar epithelium of the endometrium into stratified squamous epithelium.
(05 Mar 2000)
ichthyosis vulgaris most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
(12 Dec 1998)
ichthyosis, x-linked Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the x-chromosome and transmitted to the male offspring. It is characterised by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.
(12 Dec 1998)
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