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¿µ¹® hypothyroidism ÇÑ±Û °©»ó»ùÀúÇÏÁõ, °©»ó¼±±â´ÉÀúÇÏÁõ
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  • ¿µ¹®
    ÇѱÛ
  • hypothyroidism
    °©»ó»ùÀúÇÏÁõ, °©»ó¼±ÀúÇÏÁõ
  • infantile
    ¿µ¾Æ-
  • infantile amnesia
    ¿µ¾Æ±â±â¾ï»ó½Ç
  • infantile autism
    À¯¾ÆÀÚÆóÁõ, ¿µ¾ÆÀÚÆóÁõ
  • infantile automatism
    ¿µ¾ÆÀÚµ¿Áõ, Á¥¸ÔÀÌÀÚµ¿Áõ
  • infantile cortical hyperostosis
    ¿µ¾Æ°ÑÁú»À°ú´ÙÁõ, ¿µ¾ÆÇÇÁú°ú°ñÁõ
  • infantile dermatitis
    ¿µ¾ÆÇǺο°
  • infantile diarrhea
    ¿µ¾Æ¼³»ç
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • infantile spasm
    ¿µ¾Æ¿¬Ãà
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  • ¿µ¹®
    ÇѱÛ
  • goitrous hypothyroidism
    °©»ó»ùÁ¾°©»ó»ùÀúÇÏÁõ, ¹æÆÐ»ùÁ¾¹æÆÐ»ùÀúÇÏÁõ
  • hypothyroidism
    °©»ó»ùÀúÇÏÁõ, ¹æÆÐ»ùÀúÇÏÁõ
  • infantile amnesia
    À¯¾Æ±â±â¾ï»ó½Ç
  • infantile articulation
    ¿µ¾ÆÀÔ¼Ò¸®, ¿µ¾Æ±¸À½
  • infantile autism
    À¯¾ÆÀÚÆóÁõ, ¿µ¾ÆÀÚÆóÁõ
  • infantile automatism
    ¿µ¾ÆÀÚµ¿Áõ, Á¥¸ÔÀÌÀÚµ¿Áõ
  • infantile beriberi
    ¿µ¾Æ°¢±â
  • infantile convulsion
    ¿µ¾Æ°æ·Ã
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • Hypothyroidism
    °©»ó¼±±â´ÉÀúÇÏÁõ(Ë£ßÒàÍѦÒöî¸ù»ñø)
  • goitrous hypothyroidism
    °©»ó¼±Á¾¼º °©»ó¼±±â´ÉÀúÇÏÁõ.
  • hypothyroidism
    °©»ó¼±±â´ÉÀúÇÏÁõ, Àú°©»ó¼±±â´ÉÁõ.
  • amnesia infantile (infantile amnesia)
    À¯¾Æ±â ±â¾ï»ó½Ç.
  • Gianotti-Crosti syndrome => infantile papular acrodermatitis
    Àð³ëƼ Å©·Î½ºÆ¼ ÁõÈıº
  • Infantile digital fibromatoses
    ¿µ¾Æ¼Õ¹ß°¡¶ô ¼¶À¯Á¾Áõ
  • Kostmanns infantile genetic agraulocytosis
    ÄÚ½ºÆ®¸¸¿µ¾ÆÀ¯Àü¼º ¹«°ú¸³Áõ
  • acute anterior poliomyelitis =infantile par aly sis
    ±Þ¼º ȸ¹éô¼ö¿°(ÐáàõüéÛÜô±âÐæú).
  • hypogammaglobulinemia, infantile sex-linked
    ¼Ò¾Æ ¹Ý¼º °¨¸¶±Û·ÎºÒ¸°ÀúÇ÷Áõ
  • infantile
    À¯¾Æ, ½Å»ý¾Æ, ¼Ò¾Æ
  • infantile X-linked agammaglobulinemia
    ¹Ý¼º ¼Ò¾Æ ¹«°¨¸¶±Û·ÎºÒ¸°Áõ
  • infantile amaurotic familial idiocy
    ¿µ¾Æ¼º Èæ³»À强 °¡Á·¼º ¹éÄ¡.
  • infantile amaurotic familial idiocy
    ¿µ¾Æ¼º Èæ³»À强 °¡Á·¼º ¹éÄ¡.
  • infantile amaurotic family idiocy
    ¿µ¾ÆÈæ³»À强 °¡Á·¼º ¹éÄ¡.
  • infantile amaurotic family idiocy
    ¿µ¾ÆÈæ³»À强 °¡Á·¼º ¹éÄ¡.
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  • ¿µ¹®
    ÇѱÛ
  • goitrous hypothyroidism
    °©»ó¼±Á¾¼º °©»ó¼±±â´ÉÀúÇÏÁõ.
  • hypothyroidism
    °©»ó¼±±â´ÉÀúÇÏÁõ, Àú°©»ó¼±±â´ÉÁõ.
  • juvenile hypothyroidism
    ¿¬¼Ò¼º °©»ó¼±(±â´É)ÀúÇÏ(Áõ).
  • amnesia infantile (infantile amnesia)
    À¯¾Æ±â ±â¾ï»ó½Ç.
  • amnesia, infantile (infantile amnesia)
    À¯¾Æ±â ±â¾ï»ó½Ç.
  • 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
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hypothyroidism
    °©»ó¼±±â´ÉÀúÇÏÁõ, Àú°©»ó¼±±â´ÉÁõ
  • infantile
    ¿µ¾ÆÀÇ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
HEDH hypohidrotic ectodermal dysplasia-hypothyroidism [syndrome]
HT Hashimoto thyroiditis; hearing test; hearing threshold; heart; heart transplantation, heart transpla...
TRAP carpal tunnel syndrome, Raynaud phenomenon, aching muscles, proximal muscle weakness [rheumatic diso...
CIHS central infantile hypotonic syndrome
CINCA chronic infantile neurological cutaneous and auricular [syndrome]
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
CH Congenital Hypothyroidism
CHT Congenital hypothyroidism
EIEE Early infantile epileptic encephalopathy
IHPS Infantile Hypertrophic Pyloric Stenosis
IM Infantile Myofibromatosis
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • congenita1 hypothyroidism
    ¼±Ãµ¼º °©»ó¼± ±â´É ÀúÇÏÁõ
  • congenital hypothyroidism
    ¼±Ãµ¼º °©»ó¼± ±â´ÉÀúÇÏÁõ
  • hypothyroidism
    °©»ó¼± ±â´É ºÎÀü, °©»ó¼± ±â´É ÀúÇÏÁõ, °©»ó¼± ±â´É ºÎÀüÁõ, Àú°©»ó¼± ±â´ÉÁõ
    °©»ó¼± ±â´ÉÀÇ ÀúÇÏ·Î ÀÎÇÑ È£¸£¸óÀÇ ºÐºñ ºÎÁ·À¸·Î ÀϾ´Â ÁúȯÀ¸·Î °©»ó¼± ±â´É ºÎÀüÁõÀ̶ó°íµµ ÇÑ´Ù. ¼±Ãµ¼ºÀ̰ųª ¾î¸± ¶§ ¹ßº´Çϸé, Å©·¹Æ¾ º´
  • juvenile hypothyroidism
    À¯³â¼º °©»ó¼± ±â´É ÀúÇÏÁõ
  • transient hypothyroidism
    ÀϽÃÀû °©»ó¼± ±â´É ºÎÀüÁõ
  • aggressive infantile fibromatosis
    ħ½À À¯¾Æ ¼¶À¯Á¾Áõ
  • chronic infantile neurological cutaneous articular syndrome
    ¸¸¼º À¯¾Æ ½Å°æ ÇǺαº
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ
  • infantile ankylosis
    À¯¾Æ¼º °­Á÷
  • infantile cerebrocerebellar diplegic paralysis
    ¼Ò¾Æ³ú¼º ¾çÃø ¸¶ºñ
    ¿µ¾Æ±â¿¡ ÁøÇàÇÏ¿© »çÁö¸¦ ¸ðµÎ ħ¹üÇÏ¿©, ´ë³ú¿Í ¼Ò³úÀÇ »ó¹ÝµÇ´Â ºÎºÐÀÇ ¹ßÀ°ºÎÀüÀ̳ª ÆÄ±«ÀÇ È¥ÇÕÀ¸·Î ³ªÅ¸³­´Ù.
  • infantile eczema
    ¼Ò¾Æ½ÀÁø
    ¾î¸°À̵鿡°Ô »ý±â´Â ½ÀÁø. Á¥¸ÔÀÌ ¶§¿¡´Â ÇǺÎÀÇ ÇØºÎÀû, »ý¸®ÀûÀΠƯÀ̼ºÀ¸·Î ÀÎÇÏ¿© ½ÀÁøÀÌ ¸¹ÀÌ »ý±â´Âµ¥, ƯÈ÷ ƯÀÌÇÑ ¸ð¾çÀ» ÇϹǷΠÀ̸¦ ¼Ò¾Æ ½ÀÁøÀ̶ó°í Çϸç, Áõ¼¼¿¡ µû¶ó À¯À¯¾Æ ¾È¸é µÎºÎ ±Þ¼º ½ÀÁø, À¯¾Æ Áö·ç¼º ½ÀÁø, ¼Ò¾Æ °ÇÁ¶¼º ½ÀÁøÀÇ 3°¡Áö·Î ±¸ºÐµÈ´Ù.
  • infantile melanodontia
    ½Å»ý¾Æ Èæ»ö Ä¡¾ÆÁõ
  • infantile paralysis
    ¼Ò¾Æ ¸¶ºñ, ¼Ò¾Æ³ú¼º ¿îµ¿ ½ÇÁ¶¼º ¸¶ºñ
    µ¿ÀǾî=
  • infantile perseveration
    À¯¾Æ±â ¾ð¾îÀÇ ÀÜÁ¸
  • infantile stiff skin syndrome
    ¿µ¾Æ ÇǺΠ°æÁ÷ ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
infantile hypothyroidism <paediatrics> Stunted body growth and mental development appearing in the first years of life resulting the inappropriate development of the thymus gland or inadequate maternal intake of iodine during gestation.
(27 Sep 1997)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
congenital hypothyroidism Lack of thyroid secretion.
See: infantile hypothyroidism.
(05 Mar 2000)
secondary hypothyroidism Hypothyroidism that arises as a consequence of inadequate thyrotropin secretion by the anterior pituitary gland.
(05 Mar 2000)
hypothyroidism <endocrinology> A deficiency of thyroid activity.
In adults, it is most common in women and is characterised by decrease in basal metabolic rate, tiredness and lethargy, sensitivity to cold and menstrual disturbances. If untreated, it progresses to full blown myxoedema.
In infants, severe hypothyroidism leads to cretinism.
In juveniles, the manifestations are intermediate, with less severe mental and developmental retardation and only mild symptoms of the adult form.
When due to pituitary deficiency of thyrotropin secretion it is called secondary hypothyroidism.
(11 Jan 1998)
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)
infantile brain tumours <radiology> Can be present at birth: choroid plexus papilloma, medulloblastoma, craniopharyngioma, ependymoma, astrocytoma, teratoma
(12 Dec 1998)
infantile cataract A cataract affecting a very young child.
(05 Mar 2000)
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  • ¿µ¹®
    ÇѱÛ
  • hypothyroidism
    °©»ó¼±(±â´É)ÀúÇÏ(ºÎÀü)(Áõ)
  • infantile
    À¯¾ÆÀÇ
  • infant(infantile) prodigy
    (õÀç¾Æ,½Åµ¿)
  • infantile
    À¯¾Æ(±â)ÀÇ;¼Ò¾ÆÀÇ;¾î¸°¾ÆÀÌ °°Àº;À¯Ä¡ÇÑ;Ãʺ¸ÀÇ;õÁø³­¸¸ÇÑ
  • infantile paralysis
    ¼Ò¾Æ¸¶ºñ(Áö±ÝÀºpoliomyelitis¶ó°íÇÔ
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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