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Bardet-Biedl Syndrome

Laurence-Moon-Bardet-Biedl syndromeLaurence-Moon syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-5 of 5 results.
Clinical Registry Investigating Bardet-Biedl Syndrome
Status: Recruiting
Last Changed: Aug 11, 2020
First Received: Dec 31, 2014
Disease(s): Bardet-Biedl Syndrome
Locations: Marshfield Clinic Research Foundation, Marshfield, Wisconsin, United States
COhort for Bardet-Bield Syndrome and Alström Syndrome for Translational Research Monocentric Interventional Study
Status: Recruiting
Last Changed: Sep 25, 2020
First Received: Jul 08, 2020
Disease(s): Bardet-Biedl Syndrome, Alström Syndrome
Intervention(s): Skin biopsy
Locations: Les Hôpitaux Universitaires de Strasbourg, Strasbourg, France
GROWing Up With Rare GENEtic Syndromes
Status: Recruiting
Last Changed: Jul 09, 2020
First Received: Jul 09, 2020
Disease(s): Prader-Willi Syndrome, PWS-like Syndrome, Silver Russel Syndrome, Congenital Hypopituitarism, Klinefelter (XXY-)Syndrome, Congenital Adrenal Hyperplasia, XXXXY Syndrome, XXYY Syndrome, XXXX Syndrome (Tetra-X Syndrome), Disorders of Sex Development, Turner Syndrome, 46, XY DSD, Tuberous Sclerosis, Neurofibromatosis, Albright Hereditaire Osteodystrofie, Cornelia de Lange Syndrome, Saethre-Chotzen Syndrome, 17p- Deletiesyndrome, VCF Syndrome, POLR3A Mutatie, Ohdo Syndrome, Jacobsen Syndrome / 11 q Syndrome, Myrhe Syndrome, CHARGE Syndrome, 1q25-32 Deletie, Bardet Biedl Syndrome, Rett Syndrome, 22q11 Deletion Syndrome, Allan-Herndon-Dudley Syndrome, Kallmann Syndrome, Rare Bone Disorders, Noonan Syndrome, Williams-Beuren Syndrome
Intervention(s): Retrospective file studies
Locations: Erasmus Medical Center, Rotterdam, Zuid-Holland, Netherlands
Inherited Retinal Degenerative Disease Registry
Status: Recruiting
Last Changed: Dec 13, 2018
First Received: May 06, 2015
Disease(s): Eye Diseases Hereditary, Retinal Disease, Achromatopsia, Bardet-Biedl Syndrome, Bassen-Kornzweig Syndrome, Batten Disease, Best Disease, Choroidal Dystrophy, Choroideremia, Cone Dystrophy, Cone-Rod Dystrophy, Congenital Stationary Night Blindness, Enhanced S-Cone Syndrome, Fundus Albipunctatus, Goldmann-Favre Syndrome, Gyrate Atrophy, Juvenile Macular Degeneration, Kearns-Sayre Syndrome, Leber Congenital Amaurosis, Refsum Syndrome, Retinitis Pigmentosa, Retinitis Punctata Albescens, Retinoschisis, Rod-Cone Dystrophy, Rod Dystrophy, Rod Monochromacy, Stargardt Disease, Usher Syndrome
Locations: Foundation Fighting Blindness, Columbia, Maryland, United States
UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Status: Recruiting
Last Changed: Oct 25, 2019
First Received: Jul 26, 2011
Disease(s): Hepato/Renal Fibrocystic Disease, Autosomal Recessive Polycystic Kidney Disease, Joubert Syndrome, Bardet Biedl Syndrome, Meckel-Gruber Syndrome, Congenital Hepatic Fibrosis, Caroli Syndrome, Oro-Facial-Digital Syndrome Type I, Nephronophthisis, Glomerulocystic Kidney Disease
Locations: Children's National Health System, Washington, District of Columbia, United States