Dent disease type 2

Dent disease type 2 is a form of Dent disease that shows the kidney problems seen in Dent disease type 1 along with additional features affecting other parts of the body. The condition is characterized by its association with both renal and extra-renal manifestations, although specific extra-renal details are not extensively outlined in the available information. The information provided emphasizes that the condition shares underlying kidney-related symptoms with Dent disease type 1. This overview provides a basic understanding of the disease in terms of its clinical presentation, while recognizing that more detailed descriptions may be available in specialized medical literature.

People with Dent disease type 2 may experience kidney-related issues similar to those seen in Dent disease type 1, as well as additional symptoms affecting other parts of the body. However, detailed information about the specific symptoms and signs for this condition is limited.

Dent disease type 2 is caused by a mutation in the OCRL gene. This genetic change affects the function of cells in the kidney and other tissues and is inherited in an X-linked recessive pattern.

Information about treatment options and management approaches is currently limited for this condition.

Information about the outlook and quality of life for people with Dent disease type 2 is currently limited for this condition.

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