Muscular dystrophy
Notes: Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy ; Benign [Becker] muscular dystrophy ; Severe [Duchenne] muscular dystrophy ; Scapulohumeral muscular dystrophy ; LGMD D4 calpain-3-related ; LGMD D5 collagen 6-related ; Limb girdle muscular dystrophy type 1 ; Limb girdle muscular dystrophy type 2A ; LGMD R1 calpain-3-related ; Primary calpainopathy ; Dysferlinopathy ; LGMD R2 dysferlin-related ; Limb girdle muscular dystrophy type 2B ; Miyoshi Myopathy type 1 ; Sarcoglycanopathy, NOS ; Alpha sarcoglycanopathy ; Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency ; Limb girdle muscular dystrophy type 2D ; Beta sarcoglycanopathy ; Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency ; Limb girdle muscular dystrophy type 2E ; Delta sarcoglycanopathy ; Delta-sarcoglycan-related LGMD R6 ; Gamma sarcoglycanopathy ; Gamma-sarcoglycan-related LGMD R5 ; Limb girdle muscular dystrophy type 2C ; Limb girdle muscular dystrophy type 2F ; Anoctamin-5-related LGMD R12 ; Anoctaminopathy ; Autosomal recessive limb girdle muscular dystrophy type 2L ; Miyoshi myopathy type 3 ; LGMD R9 FKRP-related ; LGMD R22 collagen 6-related ; Limb girdle muscular dystrophy due to fukutin related protein dysfunction ; Limb girdle muscular dystrophy type 2I ; Other autosomal recessive limb girdle muscular dystrophy ; Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss] ; Congenital muscular dystrophy NOS ; Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber ; Distal muscular dystrophy ; Ocular muscular dystrophy ; Oculopharyngeal muscular dystrophy ; Scapuloperoneal muscular dystrophy
2535 แพทยศาสตร์บัณฑิต
2539 วุฒิบัตร อายุรศาสตร์
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