I, HMSN
Medical Dictionary
Definition of medical terminology for I, HMSN.
"Brainstem auditory evoked potentials and cochlear microphonics in the HMSN family with auditory neuropathy.". Pflugers Archiv: European journal of physiology 439: 204-205.. 
^ DePablos, C.; Berciano, J.; Calleja, J. (1991).
CMT, also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy, comprises a group of disorders caused by mutations in genes that affect the normal function of the peripheral nerves.
Most neurologists now consider this disorder to be one of 5 types of hereditary motor sensory neuropathy (HMSN) which simply means genetically transmitted disorder of the nerves associated with movement.
Charcot-Marie-Tooth disease (CMT), known also as Hereditary Motor and Sensory Neuropathy (HMSN), Hereditary Sensorimotor Neuropathy (HSMN), or Peroneal Muscular Atrophy, is a heterogeneous inherited disorder of nerves...
Full article ...
Charcot-Marie-Tooth hereditary neuropathy
Charcot-Marie-Tooth syndrome
CMT
hereditary motor and sensory neuropathy
HMSN
Peroneal Muscular Atrophy
PMA ...
agenesis of corpus callosum with peripheral neuropathy
agenesis of corpus callosum with polyneuropathy
Charlevoix disease
hereditary motor and sensory neuropathy with agenesis of the corpus callosum
HMSN/ACC ...
Neuroma de Morton
Neuroma Interdigital
Neuroma intermetatársico
Neuropatía Auditiva
Neuropatía Diabética
Neuropatía periferal
Neuropatías motoras y sensoriales hereditarias (HMSN)
Nistagmus
Norovirus ...
 See also: Stroke, Melanoma, Cancer, Injuries, Sclerosis
  
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