Ataxia Telangiectasia |
A-T; Louis-Bar syndrome; Telangiectasia, cerebello-oculocutaneous |
Ataxia-telangiectasia (AT) (Boder-Sedgwick syndrome or Louis-Bar syndrome) is a primary immunodeficiency disorder that occurs in an estimated incidence of 1 in 40,000 to 1 in 300,000 births (Lederman, 2000). Telangiectasias are small, red 'spider' veins. These typically appear on the surface of the ears and cheeks or in the corners of the eyes in patients with AT. The 'ataxia' part of the name refers to the difficulty patients with AT have walking. At early age, the child's walking becomes ...
Wikipedia - [full article]
Ataxia Telangiectasia Clinical Trials
- Study for Treatment of Cancer in Children With Ataxia-Telangiectasia
ClinicalTrials.gov Identifier: NCT00187057 - Recruiting
Ataxia-Telangiectasia
- Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia
ClinicalTrials.gov Identifier: NCT00202397 - Recruiting
Hereditary Ataxia; Multiple Sclerosis; Cerebellar Ataxia
- Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)
ClinicalTrials.gov Identifier: NCT00004306 - Recruiting
Hereditary Ataxia
- Ranibizumab in Idiopathic Parafoveal Telangiectasia (RIPT) Trial
ClinicalTrials.gov Identifier: NCT00378196 - Recruiting
Telangiectasia
- Idebenone to Treat Friedreich's Ataxia
ClinicalTrials.gov Identifier: NCT00229632 - Active, not recruiting
Friedreich Ataxia
- Investigation of Plasma Proteins in Patients With Hereditary Haemorrhagic Telangiectasia and PAVMs
ClinicalTrials.gov Identifier: NCT00230672 - Recruiting
Telangiectasia, Hereditary Hemorrhagic
- Case Notes Review on Patients With Hereditary Haemorrhagic Telangiectasia
ClinicalTrials.gov Identifier: NCT00230685 - Recruiting
Telangiectasia, Hereditary Hemorrhagic
- Molecular Studies on Hereditary Haemorrhagic Telangiectasia Families
ClinicalTrials.gov Identifier: NCT00230620 - Recruiting
Telangiectasia, Hereditary Hemorrhagic
- Characteristics of Episodic Ataxia Syndrome
ClinicalTrials.gov Identifier: NCT00266760 - Recruiting
Ataxia; Cerebellar Diseases
- Iron-Chelating Therapy and Friedreich Ataxia
ClinicalTrials.gov Identifier: NCT00224640 - Active, not recruiting
Friedreich Ataxia
- Ranibizumab to Treat Type 2 Idiopathic Macular Telangiectasia (RAMA-Trial)
ClinicalTrials.gov Identifier: NCT00504400 - Recruiting
Type 2 Idiopathic Macular Telangiectasia
- Transitional Life Events in Patients with Friedreich's Ataxia: Implications for Genetic Counseling
ClinicalTrials.gov Identifier: NCT00056186 - Completed
Friedreich Ataxia
- Study to Assess the Efficacy, Safety and Tolerability of Idebenone in the Treatment of Friedreich's Ataxia
ClinicalTrials.gov Identifier: NCT00537680 - Not yet recruiting
Friedreich's Ataxia
- A Study Investigating the Safety and Tolerability of Deferiprone in Patients With Friedreich's Ataxia
ClinicalTrials.gov Identifier: NCT00530127 - Not yet recruiting
Friedreich's Ataxia
- Injected Ranibizumab to Treat Macular Telangiectasia With New Blood Vessel Formation
ClinicalTrials.gov Identifier: NCT00457067 - Completed
Telangiectasia
- Injected Ranibizumab to Treat Macular Telangiectasia Without New Blood Vessel Formation
ClinicalTrials.gov Identifier: NCT00457145 - Completed
Telangiectasia
- Study of the Natural History and Genotype-Phenotype Correlations of Hereditary Hemorrhagic Telangiectasia Patients
ClinicalTrials.gov Identifier: NCT00004649 - Completed
Hereditary Hemorrhagic Telangiectasia
- Safety Study of Idebenone to Treat Friedreich's Ataxia
ClinicalTrials.gov Identifier: NCT00015808 - Completed
Friedreich Ataxia
- Investigation of Coagulation Parameters in Hereditary Haemorrhagic Telangiectasia
ClinicalTrials.gov Identifier: NCT00230659 - Completed
Telangiectasia, Hereditary Hemorrhagic
- Intravitreal Bevacizumab for Idiopathic Perifoveal Telangiectasia
ClinicalTrials.gov Identifier: NCT00451763 - Recruiting
Retina; Telangiectasis
- Phase II Pilot Study of Octreotide, a Somatostatin Octapeptide Analog, for Gastrointestinal Hemorrhage in Hormone-Refractory Hereditary Hemorrhagic Telangiectasia and Senile Ectasia
ClinicalTrials.gov Identifier: NCT00004327 - Completed
Hereditary Hemorrhagic Telangiectasia; Ectasia
- Anti-Estrogen Therapy for Hereditary Hemorrhagic Telangiectasia A Double-Blind Placebo-Controlled Clinical Trial
ClinicalTrials.gov Identifier: NCT00375622 - Completed
Hereditary Hemorrhagic Telangiectasia
- Treatment of Idiopathic Perifoveal Telangiectasia (IPT) With Open-Label Anecortave Acetate (15mg.).
ClinicalTrials.gov Identifier: NCT00211328 - Completed
Idiopathic Perifoveal Telangiectasia
- Phase 1 Trial of Idebenone to Treat Patients with Friedreich's Ataxia
ClinicalTrials.gov Identifier: NCT00078481 - Completed
Friedreich Ataxia
- Studies of White Blood Cells Derived From HHT Patients
ClinicalTrials.gov Identifier: NCT00230633 - Recruiting
Telangiectasia, Hereditary Hemorrhagic
- Phase III Randomized, Placebo-Controlled, Crossover Study of Soy Protein Isolate for Hereditary Hemorrhagic Telangiectasia
ClinicalTrials.gov Identifier: NCT00004654 - Completed
Hereditary Hemorrhagic Telangiectasia
- Effectiveness of Rituximab in Pediatric OMS Patients.
ClinicalTrials.gov Identifier: NCT00244361 - Active, not recruiting
Opsoclonus-Myoclonus Syndrome; Opsoclonus; Myoclonus; Ataxia
- Study of Inherited Neurological Disorders
ClinicalTrials.gov Identifier: NCT00004568 - Recruiting
Ataxia; Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease
- Pulsed Dye Laser and Intense Pulsed Light (IPL) for the Treatment of Telangiectasia and Skin Redness
ClinicalTrials.gov Identifier: NCT00206921 - Recruiting
Telangiectasis; Erythema
- Gluten-Free Diet in Patients with Gluten Sensitivity and Cerebellar Ataxia
ClinicalTrials.gov Identifier: NCT00006492 - Completed
Celiac Disease; Cerebellar Ataxia; Healthy
- Thalidomide Reduces Arteriovenous Malformation Related Gastrointestinal Bleeding
ClinicalTrials.gov Identifier: NCT00389935 - Recruiting
Arteriovenous Malformation; Hereditary Hemorrhagic Telangiectasia; Hematochezia; Melena
- ATERO : A Randomised Study With Tranexamic Acid in Epistaxis of Rendu Osler Syndrome
ClinicalTrials.gov Identifier: NCT00355108 - Recruiting
Telangiectasia, Hereditary Hemorrhagic; Osler-Rendu Disease
- Studies of Hereditary Hemorrhagic Telangiectasia
ClinicalTrials.gov Identifier: NCT00004648 - Completed
Telangiectasia, Hereditary Hemorrhagic
- Treatment of Exudative and Vasogenic Chorioretinal Diseases Including Variants of Age-Related Macular Degeneration (AMD) and Other Related Maculopathy
ClinicalTrials.gov Identifier: NCT00470977 - Recruiting
Coats’ Disease; Idiopathic Perifoveal Telangiectasia; Retinal Angiomatous Proliferation; Polypoidal Vasculopathy; Pseudoxanthoma Elasticum; Pathological Myopia; Multi-Focal Choroiditis; Rubeosis Iridis
- PET Scan to Study Brain Control of Human Movement
ClinicalTrials.gov Identifier: NCT00001324 - Completed
Ataxia; Cerebrovascular Accident; Healthy; Movement Disorder; Tremor@@
- Treatment of Congenital Telangiectasia (Coat's Disease) With Open-Label Anecortave Acetate (15mg.)
ClinicalTrials.gov Identifier: NCT00211315 - Completed
Coat's Disease

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