Painful legs and moving toes syndrome
Synonyms: PLMT syndrome
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare neurologic (adult-onset) movement disorder characterized by persistent pain (unilateral or bilateral) in the feet or legs (most commonly the hemi-lower limbs) and persistant twisting, non-rhythmic, involuntary movements of one or more toes. Chronic "deep aching pulling pain" includes tingling, numbness, aching, dullness, cramp, shooting, sharp, burning, and prickling.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Painful legs and moving toes syndrome | PLMT syndrome |
| fr | Syndrome de jambes douloureuses et orteils instables | |
| de | Syndrom der schmerzenden Beine und beweglichen Zehen | PLMT-Syndrom |
| es | Síndrome de piernas dolorosas y dedos de los pies en movimiento | Síndrome PLMT |
| it | Sindrome delle gambe dolorose e del movimento delle dita dei piedi | Sindrome PLMT |
| nl | Syndroom van pijnlijke benen en bewegende tenen | PLMT-syndroom |
| pt | Síndrome das pernas doridas e dedos móveis | Síndrome PLMT |
| pl | Zespół bolesnych nóg i niespokojnych palców | = en |
| cs | Syndrom bolestivých nohou a pohyblivých prstů na nohou | = en |
| uk | Синдром болю в ногах і рухомих пальців ніг | Синдром PLMT |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G25.8 | NTBT | attributed | validated |
| MONDO | 0850049 | E | validated | |
| UMLS | C5680388 | E | validated | |
| GARD | 12706 | E | validated | |
| MedDRA | 10089938 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:102003Rare movement disorder
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 144 cases | Worldwide | Case(s) | Validated | 39585061[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 39585061[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/617440
- This record as JSON: /data/d/617440.json