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Gollop-Wolfgang complex is a very rare malformation characterized by ectrodactyly of the hand and ipsilateral bifurcation of the femur.
Features include: Hand monodactyly, Aplasia of the ulna, Split hand, and Bifid femur and 2 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Arms and legs | 3 | Hand monodactyly, Split hand, Foot monodactyly |
Bones and joints |
Estimated prevalence: 1-9 in 1,000,000 (Rare).
No clinical trials have been registered for Gollop-Wolfgang complex.
4 publications have been identified in PubMed for Gollop-Wolfgang complex. Research spans Case Report / Case Series (75%) and Epidemiology / Natural History (25%).
Kim JB (2025). [PMID: 40278527](https://pubmed.ncbi.nlm.nih.gov/40278527/). *Pediatric reports*. [Case Report / Case Series]
Seeor LM (2025). [PMID: 40321490](https://pubmed.ncbi.nlm.nih.gov/40321490/). *Indian journal of orthopaedics*. [Epidemiology / Natural History]
Lachhab A (2025). [PMID: 40809670](https://pubmed.ncbi.nlm.nih.gov/40809670/). *Cureus*. [Case Report / Case Series]
Elewee A (2025). [PMID: 40769048](https://pubmed.ncbi.nlm.nih.gov/40769048/). *International journal of surgery case reports*. [Case Report / Case Series]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 12:49 AM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Gollop-Wolfgang complex
1
Bifid femur |