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5 studies found for:    LOWE OCULOCEREBRORENAL SYNDROME
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Rank Status Study
1 Completed Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
Condition: Lowe Syndrome
Intervention:
2 Completed Study of the Pathophysiological Mechanisms Involved in Bleeding Events
Condition: Oculocerebrorenal Syndrome
Intervention: Other: Blood sample
3 Recruiting Prospective Research Rare Kidney Stones (ProRKS)
Conditions: Hyperoxaluria;   Cystinuria;   Dent Disease;   Lowe Syndrome;   Adenine Phosphoribosyltransferase Deficiency
Intervention:
4 Active, not recruiting Clinical and Molecular Investigations Into Ciliopathies
Conditions: Autosomal Recessive Polycystic Kidney Disease;   Congenital Hepatic Fibrosis;   Caroli's Disease;   Polycystic Kidney Disease;   Joubert Syndrome;   Cerebro-Oculo-Renal Syndromes;   COACH Syndrome;   Senior-Loken Syndrome;   Dekaban-Arima Syndrome;   Cogan Oculomotor Apraxia;   Nephronophthisis;   Bardet-Biedl Syndrome;   Alstrom Syndrome;   Oral-Facial-Digital Syndrome
Intervention:
5 Completed Dent Disease Mutation Genotyping
Condition: Dent Disease
Intervention: Genetic: Genetic Analysis

Study has passed its completion date and status has not been verified in more than two years.