Dense deposit disease
- Glomerulonephritis membranoproliferative type 2
- Membranoproliferative glomerulonephritis type 2
- Membranoproliferative glomerulonephritis type II
- Mesangiocapillary glomerulonephritis type 2
Some people with DDD develop a buildup of yellowish deposits called drusen in the retina of the eye. These deposits usually appear in childhood or adolescence and can cause vision problems later in life. The long-term risk of vision problems in people with DDD is about 10% (1 in 10).
DDD can sometimes be associated with other conditions that are not related to kidney function. For example, it can occur with acquired partial lipodystrophy (APL), a condition characterized by a lack of fatty tissue under the skin of the upper body. In people with APL, the loss of fat in the upper body usually occurs several years before kidney disease starts.
The Human Phenotype Ontology provides the following list of signs and symptoms for Dense deposit disease. If the information is available, the table below includes how often the symptom is seen in people with this condition. You can use the MedlinePlus Medical Dictionary to look up the definitions for these medical terms.
The Human Phenotype Ontology (HPO) has collected information on how often a sign or symptom occurs in a condition. Much of this information comes from Orphanet, a European rare disease database. The frequency of a sign or symptom is usually listed as a rough estimate of the percentage of patients who have that feature.
The frequency may also be listed as a fraction. The first number of the fraction is how many people had the symptom, and the second number is the total number of people who were examined in one study. For example, a frequency of 25/25 means that in a study of 25 people all patients were found to have that symptom. Because these frequencies are based on a specific study, the fractions may be different if another group of patients are examined.
Sometimes, no information on frequency is available. In these cases, the sign or symptom may be rare or common.
- Dense deposit disease. Genetics Home Reference. February 2011; http://ghr.nlm.nih.gov/condition/dense-deposit-disease. Accessed 12/12/2014.
- Corchado JC, Smith RJH. Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II. GeneReviews. May 19, 2011; http://www.ncbi.nlm.nih.gov/books/NBK1425/. Accessed 12/12/2014.