Gollop-Wolfgang complex

From WikiMD's Wellness Encyclopedia


=Gollop-Wolfgang Complex = Gollop-Wolfgang Complex is a rare congenital disorder characterized by limb malformations and other skeletal abnormalities. It is a type of limb reduction defect that primarily affects the lower extremities.

Clinical Features[edit | edit source]

The main clinical features of Gollop-Wolfgang Complex include:

Diagnosis[edit | edit source]

Diagnosis of Gollop-Wolfgang Complex is primarily based on clinical examination and imaging studies. Radiography is used to assess the extent of limb malformations. Genetic testing may be conducted to rule out other syndromes with overlapping features.

Etiology[edit | edit source]

The exact cause of Gollop-Wolfgang Complex is not well understood. It is believed to result from disruptions in limb development during embryogenesis. There is no known genetic mutation specifically associated with this condition, and most cases appear to occur sporadically.

Differential Diagnosis[edit | edit source]

Conditions that may be considered in the differential diagnosis include:

Management[edit | edit source]

Management of Gollop-Wolfgang Complex is multidisciplinary and may involve:

Prognosis[edit | edit source]

The prognosis for individuals with Gollop-Wolfgang Complex varies depending on the severity of the limb malformations and the presence of any associated anomalies. With appropriate management, many individuals can achieve a good quality of life.

Research and Future Directions[edit | edit source]

Research into the genetic and developmental pathways involved in Gollop-Wolfgang Complex is ongoing. Understanding the molecular basis of this condition may lead to improved diagnostic and therapeutic strategies.

See Also[edit | edit source]

External Links[edit | edit source]

NIH genetic and rare disease info[edit source]

Gollop-Wolfgang complex is a rare disease.

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Contributors: Prab R. Tumpati, MD