Arthrochalasia Ehlers-Danlos syndrome
GPTKB entity
Statements (52)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:computer
|
| gptkbp:associated_with |
gptkb:historical_event
gptkb:computer anxiety fatigue sleep disturbances vision problems cardiovascular issues skin conditions neurological symptoms musculoskeletal disorders osteoporosis autoimmune disorders chronic infections endocrine disorders hernias scoliosis dental issues gastrointestinal problems dysautonomia impaired wound healing CO L1 A1 gene CO L1 A2 gene POTS (Postural Orthostatic Tachycardia Syndrome) hearing issues |
| gptkbp:caused_by |
joint hypermobility
|
| gptkbp:current_use |
joint dislocations
classical Ehlers-Danlos syndrome vascular Ehlers-Danlos syndrome |
| gptkbp:descendant |
autosomal dominant
|
| gptkbp:first_described_by |
gptkb:1998
|
| https://www.w3.org/2000/01/rdf-schema#label |
Arthrochalasia Ehlers-Danlos syndrome
|
| gptkbp:impact |
chronic pain
mobility issues psychosocial challenges |
| gptkbp:is_popular_in |
rare
|
| gptkbp:manager |
multidisciplinary approach
|
| gptkbp:research_focus |
genetic mutations
collagen synthesis connective tissue disorders |
| gptkbp:social_responsibility |
genetic testing
physical examination family history clinical evaluation |
| gptkbp:symptoms |
muscle weakness
fragile skin skin hyperelasticity |
| gptkbp:treatment |
gptkb:hospital
physical therapy pain management |
| gptkbp:bfsParent |
gptkb:computer
|
| gptkbp:bfsLayer |
3
|