A diagnosis of Dejerine-Roussy syndrome was made, but chiropractic care was considered inappropriate for the condition. Medical treatment is usually by amitriptyline and carbamezapine, but is not always successful. The prognosis is poor, with no resolution and reports of suicide in severe cases....
The affected in family 1 had early onset and severe symptoms compatible with Dejerine-Sottas syndrome (DSS), while affected in family 2 and 3 had late... GJ Braathen - 《Acta Neurologica Scandinavica》 被引量: 77发表: 2012年 Effect of oral curcumin on Dejerine-Sottas disease Curcumin is th...
Fluctuating symptoms in different parts of the body may be caused by multiple sclerosis. Sudden paralysis is most often caused by injury or stroke. Spreading paralysis may indicate degenerative disease, inflammatory disease such as Guillain-Barré syndrome or CIDP, metabolic disorders, or inherited ...
Introduction Dejerine-Roussy Syndrome (DRS), also known as central post-stroke pain, is an unusual neuropathic pain syndrome in the central nervous system. Symptoms can originate from any vascular lesion or disease affecting the central somatosensory system. Most frequently the etiology is due to ...
Conclusions: Amitriptyline is effective in treating Thalamic Pain Syndrome in an acute setting however additional studies are needed to evaluate the efficacy of the treatment. These patients need to be monitored closely as the initial symptoms can progress into severe and chronic pai...
Dejerine–Sottas syndrome is a hypertrophic, demyelinating neuropathy which appears to demonstrate autosomal recessive inheritance in most pedigrees. Clinical symptoms are similar but more severe than Charcot–Marie–Tooth disease type 1 (CMT1), of which the major subtype, CMT1 A, results either from...
SYMPTOMSMYELINATED nerve fibersIn a patient affected with a slowly progressive, severe form of Dejerine-Sottas syndrome, symmetric enlargement of cranial nerves and focal hypertrophy of cervical and caudal roots were detected following MRI. Neuropathological features of the sural nerve disclosed a ...
Objective: Describe an atypical case of ipsilateral Dejerine-Roussy syndrome(DRS) after an ischemic stroke.Background: Post-stroke thalamic pain was first described in 1906 by Joseph Dejerine and Gustave Roussy. Allodynia and tingling are the most frequent symptoms described. Anatomically, sensory ...
Germline mosaicism of MPZ gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis. Neuromuscul Disord 1999; 9: 232±8.Takashima H, Nakagawa M, Kanzaki A, et al. Germline mosaicism of MPZ gene in Dejerine–Sottas syndrome (HMSN III) associated with hereditary s...
Déjérine‐Sottas syndrome (DSS), or hereditary motor and sensory neuropathy (HMSN) type III, is a severe hypertrophic demyelinating neuropathy with infantile onset. The clinical symptoms are similar to those found in Charcot‐Marie‐Tooth disease type 1 (CMT1) or HMSN type I patients, bu...