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  • ¿µ¹®
    ÇѱÛ
  • infantile diplegia
    ¿µ¾Æ¾çÃø¸¶ºñ
  • infantile dwarf
    ¿µ¾ÆÇü³­ÀïÀÌ
  • infantile eczema
    ¿µ¾Æ½ÀÁø
  • infantile esotropia
    ¿µ¾Æ³»»ç½Ã
  • infantile gluteal granuloma
    ¿µ¾Æ¾ûµ¢À°¾ÆÁ¾, ¿µ¾ÆµÐºÎÀ°¾ÆÁ¾
  • infantile hepatitis
    ¿µ¾Æ°£¿°
  • infantile hernia
    ¿µ¾ÆÅ»Àå
  • infantile myxedema
    ¿µ¾ÆÁ¡¾×ºÎÁ¾
  • infantile neuroaxonal dystrophy
    ¿µ¾Æ½Å°æÃà»èµð½ºÆ®·ÎÇÇ
  • infantile paralysis
    ¿µ¾Æ¸¶ºñ
  • infantile pelvis
    ¿µ¾ÆÇü°ñ¹Ý
  • infantile personality
    ¿µ¾ÆÀΰÝ
  • infantile reflex
    ¿µ¾Æ¹Ý»ç
  • infantile roseola
    ¿µ¾ÆÀå¹ÌÁø
  • infantile scurvy
    ¿µ¾Æ±«Ç÷º´
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  • ¿µ¹®
    ÇѱÛ
  • infantile dermatitis
    ¿µ¾ÆÇǺο°
  • infantile diarrhea
    ¿µ¾Æ¼³»çÁõ
  • infantile diplegia
    ¿µ¾Æ¾çÃø¸¶ºñ
  • infantile dwarf
    ¿µ¾Æ³­ÀåÀÌ
  • infantile neuroaxonal dystrophy
    ¿µ¾Æ½Å°æÃà»èÅðÇàÀ§Ãà
  • epidemic infantile paralysis
    À¯Çà¼Ò¾Æ¸¶ºñ
  • infantile eczema
    ¿µ¾Æ½ÀÁø
  • infantile esotropia
    ¿µ¾Æ³»»ç½Ã
  • infantile gluteal granuloma
    ¿µ¾Æ¾ûµ¢À°¾ÆÁ¾
  • infantile hemiplegia
    ¿µ¾Æ¹Ý¸¶ºñ
  • infantile hepatitis
    ¿µ¾Æ°£¿°
  • infantile hernia
    ¿µ¾ÆÅ»Àå
  • infantile cortical hyperostosis
    ¿µ¾Æ°ÑÁú»À°ú´ÙÁõ
  • infantile sex-linked hypogammaglobulinemia
    ¼Ò¾Æ¹Ý¼ºÀú°¨¸¶±Û·ÎºÒ¸°Ç÷Áõ
  • infantile systemic hyalinosis
    À¯¾ÆÀü½ÅÀ¯¸®ÁúÁõ
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    ÇѱÛ
  • infantile articulation
    ¿µ¾Æ¼º ±¸À½
  • infantile autism
    ¿µ¾ÆÀÚÆó(Áõ)(?ä®í»øÍñø).
  • infantile autism
    À¯(¿µ)¾ÆÀÚÆó(Áõ)(êê(çÂ)ä®í»øÍñø)
  • infantile automatism
    ¿µ¾ÆÀÚµ¿Áõ, Á¥¸ÔÀÌÀÚµ¿Áõ.
  • infantile automatism
    À¯(¿µ)¾ÆÀÚµ¿Áõ,Á¥¸ÔÀÌÀÚµ¿Áõ
  • infantile beriberi
    ¿µ¾Æ°¢±â(?ä®ÊÅѨ).
  • infantile beriberi
    ¿µ¾Æ°¢±â( ä®ÊÅѨ).
  • infantile cataract
    ¿µ¾Æ±â¹é³»Àå
  • infantile cerebral paralysis
    ¿µ¾Æ(¼º) ³ú¼º¸¶ºñ(?ä®àõÒààõØ«Ýö).
  • infantile convulsion
    ¿µ¾Æ°æ·Ã.
  • infantile convulsion
    À¯(¿µ)¾Æ°æ·Ã
  • infantile cortical hyperostosis
    ¿µ¾Æ°ñ¸·ÇÇÁúÁõ½ÄÁõ.
  • infantile cortical hyperostosis
    ¿µ¾Æ ÇÇÁú¼º °ú°ñÁõ(~ä®ù«òõàõΦÍéñø), ¿µ¾Æ°ñ¸·ÇÇÁúÁõ½ÄÁõ.
  • infantile dermatitis
    ¿µ¾ÆÇǺο°.
  • infantile dermatitis
    ¿µ¾ÆÇǺο°
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    ÇѱÛ
  • tetany
    Åן´Ï, °­Ãà(Áõ)
  • tetany
    Åן´Ï, °­Ãà(Áõ).
  • acute anterior poliomyelitis =infantile par aly sis
    ±Þ¼º ȸ¹éô¼ö¿°(ÐáàõüéÛÜô±âÐæú).
  • aggressive infantile fibromatosis
    ħ½À À¯¾Æ(öÕã©àõ êáä®) ¼¶À¯Á¾Áõ(àéë«ðþñø)
  • chronic infantile neurological cutaneous articular syndrome
    ¸¸¼º À¯¾Æ ½Å°æ ÇǺΰüÀý ÁõÈıº
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ.
  • digital infantile fibromatosis
    ¼Õ¹ß°¡¶ô À¯¾Æ ¼¶À¯Á¾Áõ
  • early infantile autism
    Á¶±âÀ¯¾ÆÀÚÆóÁõ, Á¶±â¼Ò¾ÆÀÚÆóÁõ(¡­á³ä®í»øÍñø).
  • early infantile autism
    Á¶±âÀ¯¾ÆÀÚÆóÁõ(º´)(¡­í»øÍñø).
  • eczema infantile =e. infantum<³ª>
    ¿µ¾Æ ½ÀÁø.
  • epidemic infantile paralysis =p. infantills epidemica<³ª>
    À¯Ç༺ ¼Ò¾Æ¸¶ºñ.
  • hypogammaglobulinemia, infantile sex-linked
    ¼Ò¾Æ ¹Ý¼º °¨¸¶±Û·ÎºÒ¸°ÀúÇ÷Áõ
  • hypoplasia (infantile uterus)
    Çü¼ººÎÀü (À¯¾ÆÇüÀÚ±ÃÁõ)
  • infantile
    À¯¾Æ, ½Å»ý¾Æ, ¼Ò¾Æ
  • infantile X-linked agammaglobulinemia
    ¹Ý¼º ¼Ò¾Æ ¹«°¨¸¶±Û·ÎºÒ¸°Áõ
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FIMG familial infantile myasthenia gravis
IA ibotenic acid; immune adherence; immunoadsorbent; immunobiologic activity; impedance angle; indolami...
IAFI infantile amaurotic familial idiocy
IBSN infantile bilateral striated necrosis
ICP incubation period; indwelling catheter program; infantile cerebral palsy; infection-control practiti...
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INCL Infantile neuronal ceroid lipofuscinosis
IS Infantile spasm
LINCL Late infantile neuronal ceroid lipofuscinosis
I.A. infantile autism
ICP infantile cerebral paralyses
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    ÇѱÛ
    ¼³¸í
  • infantile swallow
    À¯¾Æ¼º ¿¬ÇÏ
  • infantile tooth
    À¯Ä¡
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tetany cataract A cataract that develops in hypocalcaemia.
(05 Mar 2000)
tetany of alkalosis Tetany due to a loss of acid from the body or an increase in alkali, resulting in a reduction of ionised calcium in plasma and body fluids, e.g., hyperventilation tetany (loss of CO2), gastric tetany (loss of HCl by vomiting), or injection or ingestion of excessive amounts of sodium bicarbonate.
(05 Mar 2000)
transport tetany An acute disease seen in cattle and sheep during and shortly after shipping; it appears most often in females in advanced pregnancy and is believed to be precipitated by stress, lack of food and water, and perhaps heat.
Synonym: railroad disease, railroad sickness.
(05 Mar 2000)
epidemic tetany An acute epidemic form of tetany, of several weeks' duration, occurring chiefly in winter.
Synonym: epidemic tetany.
(05 Mar 2000)
latent tetany A rather vague disorder recognised more in Europe than in the U.S. Consisting of a number of non-specific complaints, including generalised weakness, hand and foot cramping, distal paresthesia, anxiety, and depression. Some think it is a "normocalcaemic tetany"; others consider it "chronic hyperventilation syndrome." Typically with certain provoking procedures (e.g., limb ischemia, hyperventilation) in which case, obvious tetany develops.
See: Trousseau's sign, Chvostek's sign, Erb sign.
Synonym: crytotetany, spasmophilia.
(05 Mar 2000)
aggressive infantile fibromatosis A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize.
(05 Mar 2000)
autism, infantile A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment.
(12 Dec 1998)
progressive infantile spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
spasms, infantile Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth.
(12 Dec 1998)
supravalvar aortic stenosis-infantile hypercalcaemia syndrome <syndrome> Supravalvar aortic stenosis associated with elfin facies, mental retardation, and hypercalcaemia; usually sporadic; perhaps an irregular dominant trait.
(05 Mar 2000)
diffuse infantile familial sclerosis <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia
Synonym: Krabbe leukodystrophy
(12 Dec 1998)
infantile Pertaining to an infant or to infancy.
Origin: L. Infantilis
(18 Nov 1997)
infantile acute haemorrhagic oedema of the skin A generally benign form of cutaneous vasculitis, characterised by ecchymotic purpura, often in a cockade pattern, and inflammatory oedema in infants.
(05 Mar 2000)
infantile autism 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)
infantile beriberi Beriberi appearing in a breast-fed infants whose mother has beriberi due to thiamin deficiency. It is mainly the "wet" form of beriberi, characterised by heart failure with marked peripheral oedema (which is otherwise unusual in heart failure in infancy). An often fatal disease, acute in onset, which was formerly common in the Far Eastern countries where rice is consumed; reversible with thiamin.
(05 Mar 2000)
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