risque (1) surveillance (1) malformation (1) variation génétique (1) gène (1) Monitoring (1) Diagnosis (1) Causes (1) Diseases (1) Abnormalities (1) Phenotype (1) Genes (1) Dysplasia (1) Will (1) Risk (1) Reproduction (1) Prognosis (1) Patients (1) Parents (1) Human beings (1) Kidneys--Diseases (1) Human chromosome abnormalities--Diagnosis (1) Families (1) Eye (1) Example (1) Diseases (1) Diagnosis (1) Counseling (1) Coma (1) Cerebellar peduncles (1)