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Hereditary Sensory Motor Neuropathy: more detail

Hereditary Motor and Sensory Neuropathy: Webster's Timeline History, 1980 - 2007 by Icon Group International, 2009-04-16
Genetics of hereditary motor and sensory neuropathy and the Costa Rican contribution.(Charcot-Marie-Tooth (CMT)): An article from: Revista de Biología Tropical by Alejandro Leal, 2004-09-01
Charcot-Marie-Tooth Disease: A Practical Guide. Also Known as Hereditary Motor and Sensory Neuropathy and Peroneal Muscular Atrophy. by (No Author), 2000
21st Century Complete Medical Guide to Charcot-Marie-Tooth Disease (CMT), Hereditary Motor and Sensory Neuropathy (HMSN), Peroneal Muscular Atrophy, Authoritative ... for Patients and Physicians (CD-ROM) by PM Medical Health News, 2004-03
Lipidoses: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Tish, A.M. Davidson, Altha Edgren, 2006

lists with details

Peripheral Neuropathy
hereditary motorsensory neuropathy (HMSN), Sarnat, HB hereditary motor sensory Neuropathies.In Textbook of Pediatrics, ed. WE Nelson, et al., 1758-1759. 1996.
http://www.athenadiagnostics.com/site/content/diagnostic_ed/neuro_disorders/peri

Extractions: Peripheral neuropathy (PN) affects two million people in the U.S., typically middle-aged and elderly individuals. It is a neurological disorder that affects the sensory, motor and/or autonomic nerves, and is caused by abnormal function of these nerves due to various etiologies. These disorders can originate from numerous causes, such as diabetes, alcoholism, HIV, toxin exposure, metabolic abnormalities, vitamin deficiency, or adverse effects of certain drugs. However, after evaluations for the etiologies of these PNs are performed, 32-70% of all peripheral neuropathies remain idiopathic. With the development of autoimumme and genetic tests, these idiopathic peripheral neuropathies can often be diagnosed. Autoimmune Peripheral Neuropathy Symptoms of an autoimmune peripheral neuropathy may include weakness, cramping, decreased tendon reflexes, numbness, tingling, and pain affecting the arms and/or legs. Clinically, peripheral neuropathies are classified according to various characteristics: symmetric or asymmetric, proximal or distal, acute or chronic, slowly progressive or rapid onset, affecting one (mononeuropathy) or many nerves (polyneuropathy). Upon electrophysiological examination, assessment of a neuropathy can be further classified, depending on which part of the peripheral nervous system is affected, such as the axon or myelin sheath. Peripheral neuropathy can be demyelinating, axonal, or both, as determined by electromyography (EMG) and nerve conduction studies (NCS).
Neurogenetics - Hereditary Motor-Sensory Neuropathies (HMSN)
Neurogenetics hereditary motor-sensory Neuropathies (HMSN). RequestReprint, Felice, KJ et al., hereditary neuropathy with Liability
http://www.athenadiagnostics.com/site/content/diagnostic_ed/references/hmsn.asp

Extractions: Reprint Felice, K.J. et al., Hereditary Neuropathy with Liability to Pressure Palsies in Children. Pediatric Neurology 1999; 21:818-821. Chapon, F.P. et al., Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene. Journal of Neurology, Neurosurgery, and Psychiatry 1999; 66:779-782. England, J.D. Entrapment Neuropathies. Current Opinion in Neurology 1999; 12:597-602. Scherer, S.S. and Fischbeck, K.H. Is CMTX an axonopathy? Neurology 1999; 52:432. Parnell, K.J. and Pourmand, R. Evaluation of a Patient Presenting with Foot Drop. Journal of Clinical Neuromuscular Disease 1999; 1(1):41-46. N/A Scherer, S.S. Axonal Pathology in Demyelinating Diseases. Neurology 1999; 1:6-7. Request
HONselect - Hereditary Motor And Sensory Neuropathies
sensory Neuropathies, Dejerine-Sottas Disease - HMSN - HMSN Type III - HMSN TypeVII - hereditary, Type III, motor and sensory neuropathy - hereditary, Type
http://www.hon.ch/HONselect/RareDiseases/C10.500.300.html
A Case Of Motor Sensory Neuropathy
COMMENT Although the clinical and EMG evidence for hereditary sensory and motorneuropathy is overwhelming , the degree of neurogenic atrophy present in this
http://neuro-www.mgh.harvard.edu/forum/MovementDisordersF/8.23.984.52PMAcaseofMo

Extractions: My sister, Chhavi Agarwal, born 18th July,1979 is suffering from a neurological disorder which even the best neurologists in India have not been able to diaganose exactly. They have called it hereditary motor sensory neuropathy although they have not been able to match all the manifestations with any other previously known case. I would request you to spare a little of your precious time to study her case and suggest any remedies or further investigations. I shall feel highly indebted for your kind gesture.
Hereditary Motor And Sensory Neuropathy - BlueRider.com
hereditary motor and sensory neuropathy listen domain availability, hereditarymotor and sensory neuropathy. hereditary motor and sensory neuropathy n.
http://hereditary_motor_and_sensory_neuropathy.bluerider.com/wordsearch/heredita

Extractions: hereditary motor and sensory neuropathy [n] a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant Synonyms: charcot-marie-tooth_disease See Also: neuropathy
Polyneuropathy With Other Specific Features
Diphtheria. Perhexilene toxicity. hereditary motor and sensory neuropathy types1 and 3. hereditary motor sensory neuropathy (CharcotMarie-Tooth disease).
http://neuroland.com/nm/pn_specific.htm

Extractions: Neuro Med Polyneuropathy with other specific features Prominent Dysautonomia Diabetes mellitus Guillain Barre Syndrome Amyloidosis - Wash Univ (familial and acquired) Vincristine induced Porphyria - Wash Univ Hereditary sensory and autonomic neuropathy HIV-related autonomic neuropathy Idiopathic pandysautonomia Paraneoplastic sensory and autonomic ganglionopathy Ataxic sensory neuropathy Paraneoplastic sensory neuronpathy - Wash Univ Nomalignant inflammatory sensory ganglionopathy Monoclonal protein-associated neuropathy cis-Platinum tocicity - Wash Univ Pyridoxine toxicity - Wash Univ Vitamin B12 deficiency Tabes dorsalis Hereditary sensory and autonomic neuropathy Friedreich's ataxia (Baylor) and other spinocerebellar ataxias Demyelinating Polyneuropathies Guillain Barre Syndrome and variants Chronic inflammatory demyelinating polyradiculoneuropathy CIDP review - Baylor Monoclonal protein-associated neuropathy ( Search for meaning in Monoclonal protein - Postgrad Med Aug 99 Osteosclerotic myeloma Diphtheria Perhexilene toxicity Hereditary motor and sensory neuropathy types 1 and 3 Hereditary neuropathy with predisposition to pressure palsies Hereditary Neuropathy Hereditary Motor Sensory Neuropathy (Charcot-Marie-Tooth disease) Hereditary neuropathy with predisposition to pressure palsies Familial brachial plexopathy Familial amyloidosis Porphyria Other rare peripheral neuropathies:
HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH DEAFNESS
Features Listed For hereditary motor AND sensory neuropathy WITH DEAFNESS.McKusick 214370. Deafness, sensorineural; High arches of
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?779
Baylor Neurology Case Of The Month
causes (HIV, Lyme, leprosy), HNPP (hereditary neuropathy with predisposition to typicallypresents with asymmetrical motor and sensory involvement and
http://www.bcm.tmc.edu/neurol/challeng/pat26/summary.html

Extractions: Diagnosis: Multifocal Motor Neuropathy with conduction block Patient #26 presented with slowly progressive asymmetrical limb weakness, atrophy, and fasciculations without evidence of sensory or upper motor neuron involvement. The pattern of weakness was primarily distal, and cranial nerves were not affected. These findings indicate a lower motor neuron syndrome or asymmetrical motor neuropathy. The differential diagnosis includes the various causes of motor neuron disease, chronic inflammatory demyelinating neuropathy, motor neuropathies, and mononeuritis multiplex. CIDP usually causes a symmetrical, distal, sensorimotor neuropathy primarily affecting the legs (though arms may be prominently affected, and proximal involvement is not unusual). Sensory symptoms are extremely common, and sensory signs are almost universal. However, rare cases of motor involvement without significant sensory signs have been described. In most cases, however, the motor involvement is symmetrical at onset and throughout the course of the disease. The clinical course is progressive with episodes of relapse. Reflexes are universally decreased and often absent. These features argue against CIDP as the cause of neuropathy in this case. The EMG/NCV findings also argue against CIDP, as motor conduction velocities are markedly slowed even in areas without conduction blocks in CIDP findings not present in this case. Mononeuritis multiplex (multiple mononeuropathies) may be caused by diabetes mellitus, vasculitis, sarcoidosis, infectious causes (HIV, Lyme, leprosy), HNPP (hereditary neuropathy with predisposition to pressure palsies), multiple nerve tumors (neurofibromatosis), and perineuromas. Clinically, mononeuritis multiplex typically presents with asymmetrical motor and sensory involvement and variable involvement of reflexes. It would be highly unusual for mononeuritis multiplex to present as a pure motor syndrome, as in this case. The long course of the disease without other accompanying features would also be highly unusual for any of the causes of multiple mononeuropathies.
DermIS / Main Menu / DOIA / Refsum Syndrome / Info
Disease, Refsum s, Hered motor/sens neuropathy IV, hereditary motor and sensoryneuropathy type IV, hereditary sensorymotor neuropathy, type 4, hereditary
http://www.dermis.net/doia/diagnose.asp?zugr=d&lang=e&diagnr=757106&topic=i
=== Sensory Nerve Neuropathies ===
one with slow nerve conduction velocities hereditary motor and sensoryneuropathy type of peripheral nerve conduction in phenotypes.
http://www.easybuy-in1.com/neuropathy/sensory_nerve_neuropathies.htm

Extractions: ... Dx 7000 TM Voltage Nerve Conduction Threshold ... sensitive. Regional sensory V-NCT: Locating Nerve Lesions with 95% accuracy ... histamines that shift nerve conduction firing ... detection of various sensory neurological impairments ... Galvani's experiments in 1791 proved that nerves are voltage sensitive. But not until the invention of the Medi-Dx 7000 TM V-NCT device, were Galvani's principle fully exploited to the measurement nerve function. Previous Current (output) methods compared... ... THRESHOLD TEST (sNCT) NONCOVERED The Current Perception Threshold/Sensory Nerve Conduction Threshold (sNCT) test is a diagnostic test used to diagnose sensory neuropathies. The device is a noninvasive test that uses transcutaneous electrical ... The Current Perception Threshold/Sensory Nerve Conduction Threshold (sNCT) test is a diagnostic test used to diagnose sensory neuropathies. The device is a noninvasive test that uses transcutaneous electrical stimuli to evoke a sensation. There is...
Penn State Faculty Research Expertise Database (FRED)
neuropathy of infancy, HMSN IV refers to REFSUM DISEASE, HMSN V refers to a conditionmarked by a hereditary motor and sensory neuropathy associated with
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D015417
Penn State Faculty Research Expertise Database (FRED)
HMSN Vs (hereditary motor and sensory neuropathy Type V), hereditary motor sensoryneuropathy with Pyramidal Signs. hereditary motor and sensory Neuropathies,
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D015419
Disease
hereditary Peripheral Neuropathies. hereditary motor and sensory neuropathy (CharcotMarie-Toothdisease) This is the most common type of inherited neuropathy.
http://www.bgsm.edu/neurology/department/diagneuro/Disease.html

Extractions: Muscle Diseases (Myopathy) Dermatomyositis (DM): DM is an auto immune muscle disease which occurs in children and adults. The cardinal sign of this disorder is the presence of a rash commonly over the upper chest and back or shoulders. Occasionally, a purplish (heliotrope) discoloration is present over the eyelids. Along with the rash, muscle weakness in the hips and shoulders is noted. The disease develops over weeks to months. The cause is unknown but involves inflammation of the blood vessels in the skin and muscle. Diagnosis is clinical with supportive evidence from blood levels of muscle enzymes ( CK or creatine kinase ), and EMG findings. Many people undergo muscle biopsy for a definitive diagnosis. The disease responds well to oral steroids but is sometimes resistant and may require treatment with azathioprine or IVIG Polymyositis (PM) PM is similar to DM but doesn't have the rash. Symptoms develop over weeks to months in most cases. The cause is usually unknown but occasionally, PM and DM are associated with cancer or rheumatoid conditions. Treatment is similar to that of DM. Drug-induced myositis: Several medications may lead to muscle damage. These include certain cholesterol lowering agents, colchicine, and ipecac.
Mirago Results : Hereditary Angioedema
Degeneration hereditary Angioedema hereditary DeafnessRetinitis Pigmentosa hereditarysensory motor neuropathy hereditary sensory neuropathy Type III ..
http://www.mirago.co.uk/scripts/qhandler.aspx?qry=Hereditary Angioedema&ass=1218
Arquivos De Neuro-Psiquiatria -
hereditary motor AND sensory neuropathy WITH CONGENITAL GLAUCOMA. The clinicalfeatures of hereditary motor and sensory neuropathy types I and II.
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1999000200004&l
Peripheral Neuropathy
hereditary hereditary motor and sensory neuropathy type 1 and 2 (CharcotMarie-Toothdisease). hereditary sensory neuropathy. hereditary dysautonomia. Porphyria.
http://www.medic8.com/healthguide/articles/peripheralneuropathy.html

Extractions: Dr Geoff Green - Physician What is it? Peripheral neuropathy is a group of conditions affecting the nerves outside the brain and spinal cord, interfering with their function. The term generally excludes single nerve lesions (mononeuropathy) due to entrapment of the nerve or trauma. The nerves at the extremities (e.g. hands and feet) are most commonly involved. The nerves affected may be sensory (touch), motor (activating the muscles) or autonomic (feeding organs and controlling sweating and blood pressure), or a combination of these types.
Cleveland Clinic > Neuroscience > What We Treat > Nerve And Muscle Disease > Per
An example of a hereditary neuropathy is CharcotMarie Tooth (CMT) diseaseor hereditary sensory and motor neuropathy (HSMN). Acquired
http://www.clevelandclinic.org/neuroscience/treat/nerve/neuropathies.htm

Extractions: Peripheral neuropathies can be hereditary (passed within families) or acquired. Hereditary neuropathies often have characteristic clinical, electrodiagnostic, and genetic markers. An example of a hereditary neuropathy is Charcot-Marie Tooth (CMT) disease or hereditary sensory and motor neuropathy (HSMN). Acquired neuropathies, on the other hand, are more common and can be more difficult to diagnose. The most common cause of acquired polyneuropathy is diabetes mellitus. Other causes include Guillain-Barre syndrome or acute inflammatory demyelinating polyradiculoneuropathy (AIDP), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), nerve compression, nutritional deficiencies, organ failure, tumors, and a variety of generalized disorders (including, but not limited to amyloidosis, connective tissue diseases, and vasculitis). Diagnosis The treatment of peripheral neuropathies depends on the underlying cause. For instance, therapy for peripheral neuropathy caused by diabetes involves control of the diabetes. A multi-disciplinary approach is used for all peripheral neuropathies, including treatment of pain and maintenance of strength and flexibility. This is accomplished by using appropriate neuropathic medications, immune-modulating agents (such as corticosteroids, azathioprine, cyclosporine, cyclophosphamide, mycophenolate, and rituximab), IVIG, therapeutic apheresis, and physical and occupational therapy.
NEUROSCIENCEnetBASE: Neuro Sciences Online
Abnormal Deposit. hereditary NEUROPATHIES hereditary motor and sensoryNeuropathies (HMSN); hereditary sensory neuropathy; hereditary
http://www.neurosciencenetbase.com/ejournals/books/book_summary/toc.asp?id=1020
Search By Disease
66 hereditary morot and sensory neutopahty IV (HMSN IV). 67 hereditary motor andsensory neuropathy (HMSN). 73 hereditary motor sensory neuropathy 2A (HMSN2A).
http://www.eddnal.com/directory/disease.php?letter=H&page=5
Neuropathy
50, group neuropathy support. 48, hereditary motor neuropathy sensory. 47, lipitorneuropathy. 44, hereditary motor neuropathy sensory type v. 42, disease neuropathy.
http://www.thebigletterlist.net/word/n-Neuropathy.html

Extractions: If you are not a member, click here to join... it's free!. Our Mission: The Neuropathy Association is a public non profit organization. ... Our Mission: The Neuropathy Association is a public non profit organization. It was established by people with neuropathy , their families and friends, to provide support and ...

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