Seckel syndrome 4

Seckel syndrome 4 is a rare genetic condition that is a type of Seckel syndrome. It is caused by a mutation in the CENPJ gene, which is important for the normal process of cell division during growth and development. This condition is one of several types of Seckel syndrome that share overlapping features due to issues with cellular development as a result of genetic changes. People with this condition may experience features characteristic to forms of Seckel syndrome, though specific details about the range and severity of these features are not fully detailed in available sources. The information presently emphasizes the genetic cause from a mutation in the CENPJ gene, and ongoing research may provide more clarity about how these genetic changes affect physical development and other aspects of health.

Information about symptoms is currently limited for this condition.

Seckel syndrome 4 is caused by a mutation in the CENPJ gene. This gene, sometimes also referred to as CPAP, plays an important role in cell division and development. When there is a mutation in this gene, it can disrupt normal body growth processes, leading to the features associated with this form of Seckel syndrome.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.