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Charcot-Marie-Tooth disease (CMT) disease takes account of a inherited diverse group of inherited neuropathies, as well as recognized hereditary motor and sensory neuropathies (HMSN).6,7 Alterations in the GDAP1 gene sequences leads to various phenotypes of CharcotMarie-Tooth (CMT) disease, and the main medical appearance of this disease is noticeably changeable in the dominant inheritance form (CMT type 2K; CMT2K), in which transporter of the GDAP1 p.R120W mutation can exhibit a wide range of clinical brutality.
To overcome this security flaw, we put forward a new CLAS scheme for the issues of integrity and privacy in HMSN. The security analysis shows that our proposed CL-AS scheme is provably secure and can meet the security requirements in HMSN.
Charcot Marie Tooth 1 (HMSN type I according to Dyck's classification), comprises the group of demyelinating peripheral neuropathies and CMT2 (HMSN type II) comprises the axonal peripheral neuropathies (3).
Human Disorders: MFN2 Mutations Causing Other Hereditary Motor and Sensory Neuropathies (HMSNs)
A variety of additional symptoms are associated with several CMT forms, leading to the identification of new subtypes of HMSNs: type V, with spastic paraparesis, type VI, with optic atrophy, and type VII, with retinitis pigmentosa .
(1,2) The disease has been reclassified as a Hereditary Motor Sensory Neuropathy (HMSN) and there are seven main subtypes with further classification among these.
There is no cure for the HMSN diseases at present, (5) and treatments are aimed at functional restoration of gait via orthoses and surgery, (3) treatment of neuropathic pain via medications, (6) and rehabilitation exercises.
The purpose of this paper is to present a case in which the Bournemouth Questionnaire is used as an outcome measure in a patient with previously diagnosis HMSN 2 who is managed with conservative treatment and rehabilitation exercises for a concurrent problem of mechanical neck and arm pain.
El grupo de neuropatias motoras y sensoriales hereditarias (HMSN) o enfermedad de Charcot-Marie-Tooth (CMT) es el padecimiento hereditario mas comun del sistema nervioso periferico.
Palabras clave: Enfermedad de Charcot-Marie-Tooth, CMT, HMSN, genetica, Costa Rica.
It is the most familiar disease within a group of conditions called Hereditary Motor and Sensory Neuropathies (HMSN).
It is the most common sickness with a bunch of symptoms also referred as Hereditary Motor and Sensory Neuropathies (HMSN).
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- HMS Venturer
- HMS Venturer
- HMSN 1
- HMSN 3
- HMSN I
- HMSN II
- HMSN II
- HMSN V