| Ectrodactyly-polydactyly syndrome | |
|---|---|
| Other names | Ectrodactyly polydactyly |
| Specialty | Medical genetics |
| Symptoms | Combination of ectrodactyly and polydactyly |
| Complications | Walking, grip |
| Usual onset | Birth |
| Duration | Life-long (ectrodactyly) but can be corrected with surgery (polydactyly) |
| Prevention | None |
| Frequency | very rare, only 4 cases have been reported in medical literature |
| Deaths | - |
Ectrodactyly-polydactyly syndrome is a very rare congenital limb malformation syndrome of genetic origin which is characterized a combination of ectrodactyly and polydactyly[1] consisting of underdeveloped/absent central rays of the hands or feet alongside postaxial polydactyly in the same limb that can range from a hypoplastic, bone-devoid extra digit to a fully developed supernumerary digit.[2] It has been described in 4 children from a single sibship in Belgium.[3]
{{cite web}}: CS1 maint: numeric names: authors list (link)
 | This genetic disorder article is a stub. You can help Wikipedia by expanding it. |
