WAGR syndrome
WAGR syndrome is a rare genetic syndrome in which affected children are predisposed to develop Wilms' tumour, aniridia, genitourinary anomalies, and intellectual disability. The "G" is sometimes instead given as "gonadoblastoma", since the genitourinary anomalies can include tumours of the gonads.
Some WAGR syndrome patients show severe childhood obesity and hyperphagia, and are categorised as WAGRO which may be associated with the coinciding loss of brain-derived neurotrophic factor a gene that is also on chromosome 11.
The condition, first described by Miller et al. in 1964 in its association with other congenital malformations, results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring genes.
It is possible for those with WAGR syndrome to develop Wilms' tumor, a rare form of kidney cancer.
Signs and symptoms
Newborn children with WAGR syndrome are soon noted to have aniridia. The clinical suspicion for WAGR may be increased with the presence of other genital anomalies, though genitourinary anomalies are not always present, particularly in girls.In older children, clinical diagnosis of the syndrome can be made when aniridia and one of the other features are present. While aniridia is rarely absent in WAGR syndrome, cases have been reported without it. Chromosomal analysis is necessary for definitive diagnosis. Other common eye defects include cataracts and ptosis. About 50% of people with WAGR syndrome develop Wilms' tumour.
Pathophysiology
WAGR syndrome is caused by a mutation on chromosome 11 in the 11p13 region. Specifically, several genes in this area are deleted, including the PAX6 ocular development gene and the Wilms' tumour gene. Abnormalities in WT1 may also cause genitourinary anomalies. Mutations in the PAX6 gene have recently been shown to not only cause ocular abnormalities, but also problems in the brain and pancreas.The gene for brain-derived neurotrophic factor, located on 11p14.1, has been proposed as a candidate gene for the obesity and excessive eating in a subset of WAGR patients. This strengthens the case for a role for BDNF in energy balance.