Distal hereditary motor neuropathy type V (original) (raw)
Distal hereditary motor neuropathy type V is a particular type of neuropathic disorder. In general, distal hereditary motor neuropathies affect the axons of distal motor neurons and are characterized by progressive weakness and atrophy of muscles of the extremities. It is common for them to be called "spinal forms of Charcot-Marie-Tooth disease (CMT)", because the diseases are closely related in symptoms and genetic cause. The diagnostic difference in these diseases is the presence of sensory loss in the extremities. There are seven classifications of dHMNs, each defined by patterns of inheritance, age of onset, severity, and muscle groups involved. Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance, weakness of the upper limbs that is progressive and s
| Property | Value |
|---|---|
| dbo:abstract | Distal hereditary motor neuropathy type V is a particular type of neuropathic disorder. In general, distal hereditary motor neuropathies affect the axons of distal motor neurons and are characterized by progressive weakness and atrophy of muscles of the extremities. It is common for them to be called "spinal forms of Charcot-Marie-Tooth disease (CMT)", because the diseases are closely related in symptoms and genetic cause. The diagnostic difference in these diseases is the presence of sensory loss in the extremities. There are seven classifications of dHMNs, each defined by patterns of inheritance, age of onset, severity, and muscle groups involved. Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance, weakness of the upper limbs that is progressive and symmetrical, and atrophy of the small muscles of the hands. (en) |
| dbo:omim | 600794 (xsd:integer) |
| dbo:synonym | dHMN V |
| dbo:thumbnail | wiki-commons:Special:FilePath/Charcot-marie-tooth_foot.jpg?width=300 |
| dbo:wikiPageID | 51696190 (xsd:integer) |
| dbo:wikiPageLength | 8521 (xsd:nonNegativeInteger) |
| dbo:wikiPageRevisionID | 1053004317 (xsd:integer) |
| dbo:wikiPageWikiLink | dbr:Electromyography dbr:Allelic dbc:Genetic_diseases_and_disorders dbr:Chromosome_7 dbr:Hereditary_spastic_paraplegia dbr:Distal_hereditary_motor_neuropathies dbr:Dominance_(genetics) dbr:Pes_cavus dbr:Charcot-Marie-Tooth_disease dbr:Motor_neuropathy dbr:Incomplete_penetrance dbr:Genetic_dominance dbr:File:Charcot-marie-tooth_foot.jpg |
| dbp:name | Distal hereditary motor neuropathy type V (en) |
| dbp:synonym | dHMN V (en) |
| dbp:wikiPageUsesTemplate | dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist |
| dct:subject | dbc:Genetic_diseases_and_disorders |
| rdf:type | owl:Thing wikidata:Q12136 dbo:Disease |
| rdfs:comment | Distal hereditary motor neuropathy type V is a particular type of neuropathic disorder. In general, distal hereditary motor neuropathies affect the axons of distal motor neurons and are characterized by progressive weakness and atrophy of muscles of the extremities. It is common for them to be called "spinal forms of Charcot-Marie-Tooth disease (CMT)", because the diseases are closely related in symptoms and genetic cause. The diagnostic difference in these diseases is the presence of sensory loss in the extremities. There are seven classifications of dHMNs, each defined by patterns of inheritance, age of onset, severity, and muscle groups involved. Type V (sometimes notated as Type 5) is a disorder characterized by autosomal dominance, weakness of the upper limbs that is progressive and s (en) |
| rdfs:label | Distal hereditary motor neuropathy type V (en) |
| owl:sameAs | wikidata:Distal hereditary motor neuropathy type V https://global.dbpedia.org/id/2cdsf |
| prov:wasDerivedFrom | wikipedia-en:Distal_hereditary_motor_neuropathy_type_V?oldid=1053004317&ns=0 |
| foaf:depiction | wiki-commons:Special:FilePath/Charcot-marie-tooth_foot.jpg |
| foaf:isPrimaryTopicOf | wikipedia-en:Distal_hereditary_motor_neuropathy_type_V |
| foaf:name | Distal hereditary motor neuropathy type V (en) |
| is dbo:wikiPageWikiLink of | dbr:List_of_neurological_conditions_and_disorders dbr:Distal_hereditary_motor_neuronopathies dbr:Charcot–Marie–Tooth_disease |
| is foaf:primaryTopic of | wikipedia-en:Distal_hereditary_motor_neuropathy_type_V |
