Coffin-Siris syndrome 7

Coffin-Siris syndrome 7 is a rare condition that is part of the Coffin-Siris syndrome spectrum. This condition is specifically linked to a mutation in the DPF2 gene, which distinguishes it from other forms of Coffin-Siris syndrome. People with this condition may experience developmental challenges, although detailed features and variability in presentation are not fully described in the available information. The summary is based on trusted sources including genetic insights from the DPF2 gene mutation and associations noted in the OMIM database (OMIM:618027).

Information about symptoms is currently limited for this condition.

Coffin-Siris syndrome 7 is caused by a mutation in the DPF2 gene. This genetic change affects how the gene functions, leading to the characteristics observed in the condition. The cause is specifically defined by the mutation in this gene, as documented in the trusted sources.

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.