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  • congenital coronary arteriovenous fistula
    ¼±Ãµ¼º °ü»óµ¿Á¤¸Æ·ç.
  • congenital cystic eye
    ¼±Ãµ³¶Æ÷¾È
  • congenital deafness
    ¼±Ãµ(¼º) ³­Ã», ¼±Ãµ(¼º) ±Í¸Ó°Å
  • congenital debility<³ª> debilitas vitae con gen ita
    ¼±Ãµ(¼º) ¾àÁú(¡­å°òõ ).
  • congenital defect
    ¼±Ãµ¼º °á¼Õ(Áõ)(¡­ÌÀáßñø).
  • congenital defect
    ¼±Ãµ°áÇÔ
  • congenital deficiency of glucuronyl transfe ra se
    ¼±Ãµ¼º ±Û·çÄí·Ð»ê Àü À§È¿¼Ò°áÇÌÁõ(¡­ï®êÈý£áÈÌÀù¹ñø).
  • congenital deformation
    ¼±Ãµ¼º ±âÇü(¡­Ñ±û¡)
  • congenital diaphragmatic hernia
    ¼±Ãµ¼º Ⱦ°Ý¸·Ç츣´Ï¾Æ<Å»Àå>.
  • congenital dilatation of colon
    ¼±Ãµ¼º °áÀåÈ®Àå(Áõ)(¡­°áÀåÈ®ÀåÁõ).
  • congenital diplegia
    ¼±Ãµ¼º ¾çÃø¸¶ºñ(¡­å»ö° Ýö).
  • congenital dislocation
    ¼±Ãµ(¼º) Å»±¸ (¡­÷­Ï¿).
  • congenital dislocation of hip
    ¼±Ãµ¼º °í°üÀý Å»±¸(¡­ÍÆÎ¼ï½÷­Ï¿).
  • congenital disorder
    ¼±Ãµ¼º Áúȯ
  • congenital disorders of the larynx
    ¼±Ãµ(¼º) ÈĵÎÁúȯ
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LEC leukoencephalitis; lower esophageal contractility
LEL lower explosive limit; lowest effect level
LEP lethal effective phase; lipoprotein electrophoresis; low egg passage; lower esophagus
LES Lambert-Eaton syndrome; Lawrence Experimental Station [agar]; local excitatory state; Locke egg seru...
LESP lower esophageal sphincter pressure
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CCA Congenital contractural arachnodactyly
CCAM Congenital cystic adenomatoid malformation of the lung
CDA II Congenital dyserythropoietic anaemia type II
CDA Congenital dyserythropoietic anemia
CDH Congenital dysplasia of the hip
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double congenital athetosis A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia.
Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome.
(05 Mar 2000)
ichthyosiform erythroderma, congenital Designation for several severe forms of ichthyosis, present at birth, that are characterised by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalised scaling. The forms include bullous (hyperkeratosis, epidermolytic), non-bullous (ichthyosis, lamellar), wet type, and dry type.
(12 Dec 1998)
toxoplasmosis, congenital Congenital infection with toxoplasma gondii characterised by lesions of the central nervous system.
(12 Dec 1998)
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