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  • hereditary optic atrophy
    À¯Àü¼º ½Ã½Å°æÀ§Ãà.
  • hereditary oral mucoepithelial dysplasia
    À¯Àü¼º ±¸°­ Á¡¸· »óÇÇ ÀÌÇü¼º
  • hereditary orotic aciduria
    À¯Àü¼º ¿À·Îƾ»ê´¢Áõ.
  • hereditary osteodystrophy
    À¯Àü¼º °ñ ÀÌ¿µ¾çÁõ
  • hereditary persistence of Hb F =HPFH
    À¯Àü¼º žÆÇ÷»ö¼ÒÁö¼Óº´(Áõ)
  • hereditary plamoplantar keratoderma
    À¯Àü¼º ¼Õ¹ß¹Ù´Ú°¢ÇÇÁõ
  • hereditary porphyria
    À¯Àü¼º Æ÷¸£ÇǸ°Áõ.
  • hereditary porphyria cutanea tarda
    À¯Àü¼º ¸¸¹ß¼º ÇǺΠÆ÷¸£ÇǸ°Áõ
  • hereditary progressive mucinous histiocytosis X
    À¯Àü¼º ÁøÇ༺ Á¡¾×¼ºÁ¶Á÷±¸Áõ
  • hereditary protocoproporphyria
    À¯Àü¼º ÇÁ·ÎÅäÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary pyloric stenosis
    À¯Àü¼º À¯¹®ÇùÂøÁõ(¡­À¯¹®ÇùÂøÁõ).
  • hereditary pyloric stenosis
    À¯Àü¼º À¯¹®ÇùÂøÁõ(¡­êëÚ¦úõó¸ñø).
  • hereditary pyropoikilocytosis
    À¯ÀüÀû ¿­¼ºº¯Çü<--ÀÌÇü>ÀûÇ÷±¸Áõ°¡(Áõ)
  • hereditary sclerosing poikiloderma
    À¯Àü¼º °æÈ­¼º ´ÙÇüÇǺÎÁõ
  • hereditary spastic paraplegia
    À¯Àü¼º ¿¬Ã༺ ´ë¸¶ºñ.
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  • temporal epilepsy
    ÃøµÎ¼º °£Áú(¡­àõÊÖòð)
  • temporal lobe epilepsy
    ÃøµÎ¿± °£Áú(ö°Ôéç¨ÊÖòð).
  • temporal lobe epilepsy
    ÃøµÎ¿±°£Áú(ö°Ôéç¨ÊÖòð)
  • temporal lobe epilepsy
    ÃøµÎ¿±°£Áú(ö°Ôéç¨ÊÖòð).
  • thalamic epilepsy
    ½Ã»ó¼º °£Áú(¡­àõÊÖòð).
  • thalamic epilepsy
    ½Ã»ó¼º °£Áú(¡­àõÊÖòð)
  • traumatic epilepsy
    ¿Ü»ó¼º °£Áú(¡­ÊÖòð).
  • traumatic epilepsy
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  • uncinate epilepsy
    ±¸È¸°£Áú(ÏÉüÞÊÖòð)
  • verbomotor epilepsy
    ´Ùº¯¼º °£Áú(Òýܪàõ ÊÖòð).
  • congenital hereditary sensorineural
    ¼±Ãµ(¼º) À¯Àü°¨°¢½Å°æ(¼º)
  • exostosis,hereditary multiple
    ´Ù¹ß¼º À¯Àü¼º
  • familial hereditary tremor
    °¡Á·¼º À¯ÀüÁøÀü(Ê«ðéàõë¶îîòèïµ).
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
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AHC Albright's Hereditary Osteodystrophy
AHO Albright's Hereditary Osteodystrophy
HCP Hereditary Copro-Porphyria; À¯Àü¼º CoproPorphyria
HEMPAS Test Hereditary Erythrocytic Multinuclearity with Positive Acidified Serum Test
HMSN Hereditary Motor-Sensory Neuropathy
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HCSMA Hereditary Canine Spinal Muscular Atrophy
HCCAA Hereditary Cystatin C Amyloid Angiopathy
HE Hereditary Elliptocytosis
HFI Hereditary Fructose Intolerance
HHT Hereditary Haemorrhagic Telangiectasia
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secondary generalised epilepsy A group of epilepsy syndromes of diverse aetiologies with diffuse or multifocal cerebral involvement. Patients typically have a variety of generalised seizure types, including tonic, atonic, myoclonic, atypical absence, and generalised tonic-clonic seizures. Partial seizures may also occur. One classic syndrome is the Lennox-Gastaut syndrome.
Synonym: symptomatic epilepsy.
(05 Mar 2000)
sensory epilepsy Focal epilepsy initiated by a somatosensory phenomenon.
(05 Mar 2000)
sensory precipitated epilepsy Seizures which are induced by peripheral stimulation; e.g., audiogenic, laryngeal, photogenic, or other stimulation.
Synonym: sensory precipitated epilepsy.
(05 Mar 2000)
sleep epilepsy Incorrect term for narcolepsy.
(05 Mar 2000)
somnambulic epilepsy Postictal automatism in which the patient walks or runs about exhibiting natural behaviour of which he or she has no subsequent remembrance.
(05 Mar 2000)
startle epilepsy A form of reflex epilepsy precipitated by sudden noises.
(05 Mar 2000)
nocturnal epilepsy An epilepsy syndrome characterised by nocturnal seizures only.
(05 Mar 2000)
supplementary motor area epilepsy A localization-related epilepsy syndrome in which seizures originate from the supplementary motor area of the mesial frontal lobe. Typical seizure semiology includes sudden bilateral tonic movements, vocalization, and preservation of consciousness. Attacks are often nocturnal.
(05 Mar 2000)
symptomatic epilepsy A group of epilepsy syndromes of diverse aetiologies with diffuse or multifocal cerebral involvement. Patients typically have a variety of generalised seizure types, including tonic, atonic, myoclonic, atypical absence, and generalised tonic-clonic seizures. Partial seizures may also occur. One classic syndrome is the Lennox-Gastaut syndrome.
Synonym: symptomatic epilepsy.
(05 Mar 2000)
diencephalic epilepsy Episodes of autonomic dysfunction presumably due to diencephalic irritation.
Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy.
(05 Mar 2000)
idiopathic epilepsy An epilepsy without evident cause; term often used to describe the genetic epilepsies.
Synonym: generalised tonic-clonic seizure.
(05 Mar 2000)
intractable epilepsy Epilepsy not adequately controlled by medication.
Synonym: pharmacoresistent epilepsy.
(05 Mar 2000)
occipital lobe epilepsy A localization-related epilepsy where seizures originate from the occipital lobe. Symptoms commonly include visual abnormalities during seizures.
(05 Mar 2000)
temporal lobe epilepsy 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.
(27 Sep 1997)
early posttraumatic epilepsy Seizures beginning within one week after severe head injury.
(05 Mar 2000)
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