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À¯³â±â ±ÙÀ§Ã༺Ãø»è°æÈ­Áõ 2¿¹ Two Cases of Juvenile Amyotrophic Lateral Sclerosis

½ÅÇý¿ø, ¾çÀçÈÆ, Á¤¿¬°æ, ±è½Â¹Î, ¼±¿ìÀϳ²,
¼Ò¼Ó »ó¼¼Á¤º¸
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

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.

Å°¿öµå

Juvenile ALS;chronic motor neuron disease

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