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  • hereditary epilepsy
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  • idiopathic epilepsy
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  • juvenile myoclonic epilepsy
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  • latent epilepsy
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  • localized epilepsy
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  • major epilepsy
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  • minor epilepsy
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  • myoclonic epilepsy
    ±Ù(À°)°£´ë°£Áú
  • neonatal epilepsy
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  • nocturnal epilepsy
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  • organic epilepsy
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  • photic epilepsy
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  • photogenic epilepsy
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  • photosensitive epilepsy
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  • post-apoplectic epilepsy
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  • hysterical epilepsy
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  • idiopathic epilepsy
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  • juvenile myoclonic epilepsy
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  • latent epilepsy
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  • local epilepsy
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  • major epilepsy
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  • masked epilepsy
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  • minor epilepsy
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  • morpheic epilepsy
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  • myoclonic epilepsy
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  • neonatal epilepsy
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  • nocturnal epilepsy
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  • organic epilepsy
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  • petit mal epilepsy
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  • photic epilepsy
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  • hepatic triglyceride lipase absence
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  • Jacksonian epilepsy
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  • abortive epilepsy
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  • affect epilepsy
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  • arithmetical epilepsy
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  • genuine epilepsy
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  • grand mal epilepsy
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  • gustatory epilepsy
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  • hereditary epilepsy
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  • hiernosus =epilepsy
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  • hysterical epilepsy
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  • petit mal epilepsy
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  • photogenic epilepsy
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  • photosensitive epilepsy
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  • postapoplectic epilepsy
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  • congenital absence
    ¼±Ãµ¼º °á¿©(Áõ) (¡­ÌÀåýñø).
  • congenital localized absence of skin
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  • hepatic triglyceride lipase absence
    °£Áß¼ºÁö¹æ ¸®ÆÄÁ¦°á¿©(Áõ)
  • longitudinal absence
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  • sickness absence
    Áúº´°á±Ù(ÊÙË­Ë»), Áúº´ÈÞ¾÷(ÊÙÌ·Ëâ).
  • terminal absence
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  • transverse absence
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  • childhood
    ¾Æµ¿±â, ¼Ò¾Æ±â.
  • childhood depression
    ¼Ò¾Æ±â ¿ì¿ïÁõ(º´)
  • childhood disintegrative disorder
    ¼Ò¾Æ±â ºØ±«¼º Àå¾Ö
  • childhood eczema
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  • childhood febrile seizure
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  • childhood or adolescence antisocial behavior
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  • childhood psychosis
    ¼Ò¾Æ±â Á¤½Åº´(Áõ)
  • childhood schizophrenia
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CAV congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat...
CBAVD congenital bilateral absence of vas deferens
CLAS congenital localized absence of skin
LOA leave of absence; Leber optic atrophy; left occipitoanterior [fetal position]
PIVKA protein induced by vitamin K absence or antagonism
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CBAVD Congenital bilateal absence of the vas deferens
or absence Presence
PIVKA-II Protein induced by vitamin K absence or antagonist II
ALSPAC Avon Longitudinal Study of Pregnancy and Childhood
BMRTC Bone metastasising renal tumour of childhood
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  • abortive epilepsy
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  • affect epilepsy
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  • akinetic epilepsy
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  • epilepsy
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  • focal epilepsy
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  • Jackson's epilepsy
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  • juvenile myoclonic epilepsy
    û¼Ò³â ±Ù °£´ë¼º °£Áú
  • myoclonic epilepsy and raggedred fibers
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  • peripheral epilepsy
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  • petit mal epilepsy
    ¼Ò¹ßÀÛ °£Áú
    ±ÙÀÇ °£´ë¼º ¿¬ÃàÀº °æµµÀÇ °Í »ÓÀÌÁö¸¸ ÀǽÄÀÇ µ¹¿¬, ¼ø°£ÀûÀÎ »ó½ÇÀÌ ÀϾ´Â °£Áú. ƯÈ÷ ¼Ò¾Æ¿¡°Ô¼­ º¼ ¼ö ÀÖ°í, ¹ßÀÛ Áß°ú °¢ ¹ßÀÛ »çÀÌÀÇ ³úÆÄ¿¡ ³ªÅ¸³ª´Â 3-c.
  • post-traumatic epilepsy
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  • temporal epilepsy
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  • traumatic epilepsy
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  • uncinate epilepsy
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CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
childhood The period of life between infancy and puberty.
(05 Mar 2000)
childhood muscular dystrophy The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females).
Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy.
(05 Mar 2000)
childhood schizophrenia A severe emotional disturbance of childhood characterised by qualitative impairment in reciprocal social interaction and in communication, language, and social development.
Synonym: autistic disorder, childhood schizophrenia, early infantile autism, Kanner's syndrome.
(05 Mar 2000)
childhood tuberculosis Initial (primary) infection with Mycobacterium tuberculosis, characterised by pneumonic lesions in middle parts of lungs, rarely cavitary, with rapid spread to lymph nodes in hilar and paratracheal areas; more often seen in childhood, but pattern is not limited to children.
(05 Mar 2000)
childhood type tuberculosis First infection by Mycobacterium tuberculosis, typically seen in children but also occurs in adults, characterised in the lungs by the formation of a primary complex consisting of small peripheral pulmonary focus with spread to hilar or paratracheal lymph nodes; may cavitate or heal with scarring or may progress.
Synonym: childhood type tuberculosis.
(05 Mar 2000)
chronic bullous dermatosis of childhood A rare self-limiting bullous disease, chiefly of the trunk, perioral, and pelvic areas, with onset in the first decade, successively less severe recurrences, and total remission at adolescence; linear epidermal basement membrane zone deposit of IgA is found in involved and in normal skin.
Synonym: linear IgA bullous disease in children.
(05 Mar 2000)
chronic granulomatous disease of childhood <radiology> Disorder of phagocytosis, two forms: X-linked recessive, autosomal recessive, usually fatal in childhood, infection by nonpathogenic organisms (catalase positive), pneumonia, osteomyelitis, diarrhoea, abdominal pain Findings: recurrent pneumonia (resolves incompletely, with abscess formation), adenopathy (big hila), hepatosplenomegaly, calcified granulomata in liver, spleen, lymph nodes, gastric antral narrowing (!) Cf: Chediak-Higashi syndrome More info: chronic granulomatous disease
(12 Dec 1998)
schizophrenia, childhood An obsolete concept, historically used for childhood mental disorders thought to be a form of schizophrenia.
(12 Dec 1998)
torsion disease of childhood A genetic, environmental, or idiopathic disorder, usually beginning in childhood or adolescence, marked by muscular contractions that distort the spine, limbs, hips, and sometimes the cranial-innervated muscles. The abnormal movements are increased by excitement and, at least initially, abolished by sleep. The musculature is hypertonic when in action, hypotonic when at rest. Hereditary forms usually begin with involuntary posturing of the foot or hand (autosomal recessive form ) or of the neck or trunk (autosomal dominant form ); both forms may progress to produce contortions of the entire body.
Synonym: progressive torsion spasm, torsion disease of childhood, torsion dystonia, Ziehen-Oppenheim disease.
(05 Mar 2000)
feeding and eating disorders of childhood Mental disorders related to feeding and eating that are usually diagnosed in infancy or early childhood.
(12 Dec 1998)
anosognosic epilepsy Epilepsy characterised by attacks of which the person is unaware.
Synonym: anosognosic seizures.
(05 Mar 2000)
automatic epilepsy <neurology> Seizures with elaborate and multiple sensory, motor, and/or psychic components.
A common feature is the clouding of consciousness and amnesia for the event. Some clinical manifestations may include more complex behaviours like burst of anger, emotional outbursts, fear or automatisms. The EEG often reveals spike discharges in the temporal lobe during sleep.
(02 Jan 1998)
autonomic epilepsy Episodes of autonomic dysfunction presumably due to diencephalic irritation.
Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy.
(05 Mar 2000)
major epilepsy tonic-clonic seizure
vasomotor epilepsy Episodes of autonomic dysfunction presumably due to diencephalic irritation.
Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy.
(05 Mar 2000)
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