Fanconi anemia complementation group G

Fanconi anemia complementation group G is a form of Fanconi anemia that is caused by mutations in the FANCG gene. People with this condition have changes in their DNA that can affect the ability of cells to repair damage. Fanconi anemia is a rare genetic disorder that can lead to a range of health issues. The condition is part of a group of disorders that share similarities in how cells respond to DNA damage, although specific symptoms and severity may vary among individuals.

Information about symptoms is currently limited for this condition.

This condition is due to mutations in the FANCG gene, which is involved in the repair of DNA damage. These genetic changes disrupt normal cell function, which can lead to the varied features seen in Fanconi anemia.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.