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Two Cases of Juvenile Amyotrophic Lateral Sclerosis
½ÅÇý¿ø, ¾çÀçÈÆ, Á¤¿¬°æ, ±è½Â¹Î, ¼±¿ìÀϳ²,
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½ÅÇý¿ø ( Shin Hae-Won )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
¾çÀçÈÆ ( Yang Jae-Hoon )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
Á¤¿¬°æ ( Jung Yeon-Kyung )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
±è½Â¹Î ( Kim Seung-Min )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
¼±¿ìÀϳ² ( Sunwoo Il-Nam )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
KMID : 0860920040060010058
Abstract
Juvenile amyotrophic lateral sclerosis (ALS) is a rarely occurring chronic motor neuron disease, characterized by combined upper and lower motor neuron symptoms /signs with the onset before 25 years old. It is known that the inheritance is either autosomal dominant, autosomal recessive or sporadic. We report 2 cases of juvenile ALS without family history who showed severe weakness in distal limbs with definite upper motor neuron signs.
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Juvenile ALS;chronic motor neuron disease
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