The Peroneal Type of Progressive Muscular Atrophy
GPTKB entity
Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
peripheral nerves
|
| gptkbp:alsoKnownAs |
gptkb:Charcot-Marie-Tooth_disease
|
| gptkbp:category |
gptkb:hereditary_spastic_paraplegia
muscular dystrophy |
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:characterizedBy |
muscle atrophy
progressive muscle weakness |
| gptkbp:diagnosedBy |
genetic testing
nerve conduction studies |
| gptkbp:firstDescribed |
gptkb:Pierre_Marie
gptkb:Jean-Martin_Charcot gptkb:Howard_Henry_Tooth |
| https://www.w3.org/2000/01/rdf-schema#label |
The Peroneal Type of Progressive Muscular Atrophy
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive X-linked |
| gptkbp:onset |
childhood
adolescence |
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
foot drop
loss of sensation in feet and legs high arched feet |
| gptkbp:treatment |
occupational therapy
physical therapy orthopedic devices |
| gptkbp:bfsParent |
gptkb:Howard_Henry_Tooth
|
| gptkbp:bfsLayer |
7
|