Gollop-Wolfgang complex is a very rare genetic disorder which is characterized by skeletal and digital anomalies.
Signs and symptoms This complex consists of the following symptoms:
Bifid femur Hypoplastic/aplastic tibia and ulnae bone Shortening of the limbs Ectrodactyly
Causes When the genome of an isolated case of Gollop-Wolfgang complex was analyzed, Asamoah et al. discovered a deletion in the long arm of chromosome 8, this deletion consisted of the absence of 8q11.23-q13.3.
Epidemiology According to OMIM, only 26 cases have been described in medical literature. According to ORPHANET, 200 cases have been reported.
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