Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome
Synonyms: Synactyly-camptodactyly and clinodactyly of fifth fingers-bifid halluces syndrome · Wahab syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Autosomal recessive
- Age of onset
- Infancy, Neonatal
- Status
- active
A rare, genetic, congenital limb malformation syndrome characterized by a unique combination of bilateral, symmetrical camptodactyly and clinodactyly of 5th fingers, mesoaxial camptodactyly of toes, and ulnar deviation of 3rd fingers. Additional variable manifestations include bifid toes and severe syndactyly, or synpolydactyly, involving all digits of hands and feet.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome | Synactyly-camptodactyly and clinodactyly of fifth fingers-bifid halluces syndrome · Wahab syndrome |
| fr | Syndrome de syndactylie-camptodactylie et clinodactylie de l'auriculaire-gros orteils bifides | Syndrome de Wahab |
| de | Syndaktylie - Kamptodaktylie und Klinodaktylie des fünften Fingers - bifide Zehen | Wahab-Syndrom |
| es | Síndrome de sindactilia-camptodactilia y clinodactilia del quinto dedo de la mano-dedos de los pies bífidos | Síndrome de Wahab |
| it | Sindattilia - camptodattilia e clinodattilia del quinto dito - dita dei piedi bifide | |
| nl | Syndactylie - camptodactylie en clinodactylie van vijfde vingers - gespleten tenen-syndroom | Syndactylie - camptodactylie en clinodactylie van vijfde vingers - gespleten halluces-syndroom · Syndroom van Wahab |
| pt | Síndrome de sindactilia-camptodactilia e clinodactilia do quinto dedo-dedos dos pés bífidos | |
| pl | Syndaktylia - kamptodaktylia i klinodaktylia piątych palców - rozszczep palców stóp | Syndaktylia - kamptodaktylia i klinodaktylia piątych palców - rozszczep dużych palców stóp · Zespół Wahaba |
| cs | Syndrom zahrnující syndaktylii, kamptodaktylii a klinodaktylii pátých prstů ruky a rozštěpení palce u nohy | Syndaktylie, kamptodaktylie a klinodaktylie pátých prstů ruky a bifidní palce · Wahabův syndrom |
| uk | Синдром синдактилії-камптодактилії та клінодактилії пятих пальців-роздвоєння пальців на ногах | Синдром синактилії-камптодактилії та клінодактилії пятих пальців - подвоєних великих пальців · Синдром Вахабу |
| zh | 并指畸形-第五指屈曲和侧弯-双足趾综合征 | Wahab综合征 |
| tr | Sindaktili-beşinci parmak kamptodaktili ve klinodaktilisi-bifid ayak sendromu | Beşinci parmak-bifid halüsis sendromunun sözdizimsel-kamptodaktili ve klinodaktili · Wahab sendromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 615170 | E | validated | |
| ICD-10 | Q87.2 | NTBT | attributed | validated |
| MONDO | 0014069 | E | validated | |
| UMLS | C3554611 | 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:294959Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone 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 | 26 cases | Worldwide | Case(s) | Validated | 20683984[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 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/357332
- This record as JSON: /data/d/357332.json