*  Repository for Inherited Eye Diseases - Full Text View - ClinicalTrials.gov
Eye Diseases. Retinitis. Retinitis Pigmentosa. Cone-Rod Dystrophies. Retinal Diseases. Eye Diseases, Hereditary. Retinal ... MedlinePlus related topics: Eye Care Eye Diseases Genetic and Rare Diseases Information Center resources: Retinitis Pigmentosa ... Disease-causing mutations are associated with many eye diseases, including glaucoma, cataracts, strabismus, corneal dystrophies ... Severe systemic disease that compromise the ability of the referring clinician to obtain an adequate eye examination. ...
  https://clinicaltrials.gov/ct2/show/study/NCT00378742?term=NCT00378742&rank=1&show_locs=Y
*  Mastiff | Dog Breed Health
Dogs bred to the KC's breed standards could suffer from pain, hereditary diseases and developing health problems. These ... Eye disease: Progressive retinal atrophy (PRA) (annual testing) (gradual loss of vision) ... Inherited Diseases in Dogs (IDID). University of Cambridge, Dr David Sargan, Inherited Diseases in Dogs (IDID). IDID is a ... Other Diseases Reported. (For which there are currently no genetic or screening tests for sire or dam) ...
  http://www.dogbreedhealth.com/mastiff/
*  Hereditary eye disease | Veterinary Record
You can manage your cookie settings via your browser at any time. To learn more about how we use cookies, please see our cookies policy. ...
  https://veterinaryrecord.bmj.com/collection/hereditary-eye-disease
*  FAQ • Eye Diseases, Hereditary
Hereditary. On-line free medical diagnosis assistant. Ranked list of possible diseases from either several symptoms or a full ... A similarity measure between symptoms and diseases is provided. ... eye diseases or and eye doctor who specialize in eye diseases? ... FAQ - Eye Diseases, Hereditary. (Powered by Yahoo! Answers). How to learn eye diseases, symptoms, and treatments?. I am ... how to reduce hereditary under eye bags?. hey im 14 and i have bags under my eyes. im pretty sure they are hereditary but they ...
  https://lookfordiagnosis.com/faq.php?term=Eye+Diseases%2C+Hereditary&lang=1&from=20
*  Effect of Percutaneous Botulinum Toxin A Injection on Natural Course of Upper Lid Retraction in Thyroid Eye Disease - Full Text...
Eye Diseases. Graves Ophthalmopathy. Eye Diseases, Hereditary. Graves Disease. Exophthalmos. Orbital Diseases. Goiter. Thyroid ... Endocrine System Diseases. Hyperthyroidism. Autoimmune Diseases. Immune System Diseases. Botulinum Toxins. Botulinum Toxins, ... Effect of Percutaneous Botulinum Toxin A Injection on Natural Course of Upper Lid Retraction in Thyroid Eye Disease. The safety ... In active phase of thyroid eye disease some patients have obvious upper lid retraction , and sometimes exposure keratopathy .To ...
  https://clinicaltrials.gov/ct2/show/NCT00370734?recr=Open&cond=%22Hyperthyroidism%22&rank=19
*  A Safety and Tolerability Study of Otelixizumab in Thyroid Eye Disease - Full Text View - ClinicalTrials.gov
Eye Diseases, Hereditary. Eye Diseases. Graves Ophthalmopathy. Graves Disease. Exophthalmos. Orbital Diseases. Goiter. Thyroid ... MedlinePlus related topics: Eye Diseases Thyroid Diseases Genetic and Rare Diseases Information Center resources: Graves' ... Endocrine System Diseases. Hyperthyroidism. Autoimmune Diseases. Immune System Diseases. Prednisolone acetate. ... A Safety and Tolerability Study of Otelixizumab in Thyroid Eye Disease. This study has been terminated. ...
  https://clinicaltrials.gov/ct2/show/NCT01114503?cond=%22Eye+Diseases%2C+Hereditary%22+OR+%22Peters+plus+syndrome%22&rank=17
*  Teprotumumab (RV 001) Treatment in Patients With Active Thyroid Eye Disease - Full Text View - ClinicalTrials.gov
Thyroid Diseases. Eye Diseases. Graves Ophthalmopathy. Endocrine System Diseases. Eye Diseases, Hereditary. Graves Disease. ... Teprotumumab (RV 001) Treatment in Patients With Active Thyroid Eye Disease. The safety and scientific validity of this study ... Condition or disease Intervention/treatment Phase Thyroid Associated Ophthalmopathies Thyroid-Associated Ophthalmopathy Drug: ... amount of protrusion of the eye from the orbital rim) of ≥ 2 mm in the study eye, and no deterioration (increase in CAS of ≥ 2 ...
  https://www.clinicaltrials.gov/ct2/show/NCT01868997?term=Teprotumumab&rank=4
*  The Secondary Beneficial Effects of Prostaglandin Analog Treatment in Thyroid Eye Disease Patients. - Full Text View -...
Eye Diseases. Graves Ophthalmopathy. Endocrine System Diseases. Eye Diseases, Hereditary. Graves Disease. Exophthalmos. Orbital ... The eyes with thyroid eye disease and elevated intraocular pressure will be randomised to the PA treatment and the other eye ... MedlinePlus related topics: Eye Care Eye Diseases Thyroid Diseases Drug Information available for: Thyroid Timolol Timolol ... Condition or disease Intervention/treatment Phase Thyroid Eye Disease Ocular Hypertension Glaucoma Drug: Prostaglandin Analog ...
  https://clinicaltrials.gov/ct2/show/NCT01927406?recr=Open&cond=%22Eye+Diseases%22&rank=5
*  The Secondary Beneficial Effects of Prostaglandin Analog Treatment in Thyroid Eye Disease Patients. - Full Text View -...
Eye Diseases. Graves Ophthalmopathy. Endocrine System Diseases. Eye Diseases, Hereditary. Graves Disease. Exophthalmos. Orbital ... The eyes with thyroid eye disease and elevated intraocular pressure will be randomised to the PA treatment and the other eye ... MedlinePlus related topics: Eye Care Eye Diseases Thyroid Diseases Drug Information available for: Thyroid Timolol Timolol ... In this group, with thyroid eye disease and increased intraocular pressure in only one eye Prostaglandin Analog eyedrop ( ...
  https://clinicaltrials.gov/ct2/show/NCT01927406?recr=Open&cond=%22Hyperthyroidism%22&rank=12
*  Search of: stargardt's macular dystrophy - List Results - ClinicalTrials.gov
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... Bascom Palmer Eye institute. Miami, Florida, United States. *Wills Eye Institute-Mid Atlantic Retina. Philadelphia, ... Bascom Palmer Eye institute. Miami, Florida, United States. *Wills Eye Institute-Mid Atlantic Retina. Philadelphia, ... Wilmer Eye Institute, Johns Hopkins University. Baltimore, Maryland, United States. *Cole Eye Institute, Cleveland Clinic. ...
  https://clinicaltrials.gov/ct2/results?term=stargardt
*  Search of: batten - List Results - ClinicalTrials.gov
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford. *Rare Disorders ... Natural history of disease progression. 15. All. 2 Years to 25 Years (Child, Adult). NCT03285425. IRB16-00554. Batten' ... 18 Years of Age With CLN2 Disease. *Jansky-Bielschowsky Disease ... Batten Disease Support and Research Assocation (BDSRA). Other. ...
  https://www.clinicaltrials.gov/ct2/results?term=batten&Search=Search
*  Clinical Trial of Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations - Full Text View - ClinicalTrials.gov
Retinal Diseases. Blindness. Leber Congenital Amaurosis. Eye Diseases. Vision Disorders. Sensation Disorders. Neurologic ... Complicating systemic diseases;. *Impaired coagulation or use of anti-platelet agents within 7 days prior to study agent ... Pre-existing eye conditions that would preclude the planned surgery or interfere with the interpretation of study endpoints ( ... Retinal disease caused by homozygous or compound heterozygote RPE65 mutations;. *Clinical diagnosis of Leber congenital ...
  https://clinicaltrials.gov/ct2/show/NCT00821340?cond=%22Leber+congenital+amaurosis%22+OR+%22Leber+Congenital+Amaurosis%22&rank=4
*  Search of: 'late-infantile neuronal ceroid lipofuscinosis' OR 'Jansky-Bielschowsky disease' OR 'Neuronal Ceroid-Lipofuscinoses'...
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... A Multicenter, Multi-national Open-label Program to Provide BMN 190 to Patients Diagnosed With CLN2 Disease. *CLN2 Disease ... Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford. *Rare Disorders ... Natural history of disease progression. 15. All. 2 Years to 25 Years (Child, Adult). NCT03285425. IRB16-00554. Batten' ...
  https://clinicaltrials.gov/ct2/results?cond=%22late-infantile+neuronal+ceroid+lipofuscinosis%22+OR+%22Jansky-Bielschowsky+disease%22+OR+%22Neuronal+Ceroid-Lipofuscinoses%22
*  Near-infrared Light-emitting Diode (NIR-LED) Therapy for Leber's Hereditary Optic Neuropathy (LHON) - Full Text View -...
Eye Diseases, Hereditary. Optic Nerve Diseases. Cranial Nerve Diseases. Nervous System Diseases. Eye Diseases. Optic Atrophy. ... Condition or disease Intervention/treatment Phase Leber's Hereditary Optic Neuropathy (LHON) Device: Near-infrared light- ... Genetics Home Reference related topics: Leber hereditary optic neuropathy MedlinePlus related topics: Eye Care Optic Nerve ... Has an optic nerve disease other than LHON.. *Significant renal disease, defined as a history of chronic renal failure ...
  https://clinicaltrials.gov/ct2/show/NCT01389817?term=Hereditary+Neuropathies&rank=9
*  Search of: 'Kuf's disease' OR 'Neuronal Ceroid-Lipofuscinoses' - List Results - ClinicalTrials.gov
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford. *Rare Disorders ... Natural history of disease progression. 15. All. 2 Years to 25 Years (Child, Adult). NCT03285425. IRB16-00554. Batten' ... 18 Years of Age With CLN2 Disease. *Jansky-Bielschowsky Disease ... s disease, and dementias, such as Alzheimer's disease, ...
  https://clinicaltrials.gov/ct2/results?cond=%22Kuf
*  Morphometric Analysis of Orbital Structures in Graves´ Orbitopathy - Full Text View - ClinicalTrials.gov
Eye Diseases, Hereditary. Eye Diseases. Graves Disease. Exophthalmos. Orbital Diseases. Goiter. Thyroid Diseases. Endocrine ... Some changes in orbital structures detected by imaging exams could predict severity of the ocular Graves´disease. Thus the ... The purpose of this protocol is to study orbital structures in Graves´ Disease using multidetector computed tomography and ... study could be useful in improve medical management of patients with Graves´ Disease. ...
  https://clinicaltrials.gov/ct2/show/NCT00665795?recr=Open&cond=%22Graves+Disease%22&rank=13
*  Fuchs' Torsional Phaco Study - Full Text View - ClinicalTrials.gov
Corneal Dystrophies, Hereditary. Corneal Diseases. Eye Diseases. Eye Diseases, Hereditary. Genetic Diseases, Inborn. ... Fuchs' endothelial dystrophy is a progressive, bilateral disease of the corneal endothelium, which eventually leads to corneal ...
  https://clinicaltrials.gov/ct2/show/NCT00781027?cond=%22lattice+corneal+dystrophy+type+I%22+OR+%22Corneal+Dystrophies%2C+Hereditary%22&rank=11
*  Search of: 'MERRF Syndrome' OR 'Mitochondrial Myopathies' OR 'myoclonic epilepsy with ragged-red fibers' - List Results -...
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... An Observational Study of Patients With Primary Mitochondrial Disease (SPIMM-300). *Primary Mitochondrial Disease ... North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC). *Mitochondrial Disorders ... The Effects of Exercise Versus Inactivity on People With Mitochondrial Muscle Disease. *Mitochondrial Myopathy ...
  https://clinicaltrials.gov/ct2/results?cond=%22MERRF+Syndrome%22+OR+%22Mitochondrial+Myopathies%22+OR+%22myoclonic+epilepsy+with+ragged-red+fibers%22&show_rss=Y&sel_rss=mod14
*  Phase I Trial of Gene Vector to Patients With Retinal Disease Due to RPE65 Mutations - Full Text View - ClinicalTrials.gov
Eye Diseases. Vision Disorders. Sensation Disorders. Neurologic Manifestations. Nervous System Diseases. Signs and Symptoms. ... MedlinePlus related topics: Eye Care Genes and Gene Therapy Retinal Disorders Genetic and Rare Diseases Information Center ... RPE65-associated retinal disease (two disease-causing RPE65 mutations);. *Clinical diagnosis of Leber congenital amaurosis (LCA ... Phase I Trial of Gene Vector to Patients With Retinal Disease Due to RPE65 Mutations (LCA). The safety and scientific validity ...
  https://clinicaltrials.gov/ct2/show/NCT00481546?recr=Open&cond=%22Blindness%22&rank=19
*  Comparison of Two Steroid Regimens to Prevent Transplant Rejection After Corneal Transplant (DMEK) - Full Text View -...
Corneal Dystrophies, Hereditary. Fuchs' Endothelial Dystrophy. Corneal Diseases. Eye Diseases. Eye Diseases, Hereditary. ... To help prevent rejection, corticosteroid eye drops are used after transplant surgery. The steroid eye drop dosing regimen ... Condition or disease Intervention/treatment Phase Fuchs' Dystrophy Bullous Keratopathy Drug: Prednisolone acetate Drug: ... Number of Eyes With Intraocular Pressure (IOP) Elevation [ Time Frame: one day, two days, one week, one month, 3 months, 6 ...
  https://clinicaltrials.gov/ct2/show/NCT01448213?cond=%22lattice+corneal+dystrophy+type+I%22+OR+%22Corneal+Dystrophies%2C+Hereditary%22&rank=12
*  Search of: Mitochondrial Myopathies - List Results - ClinicalTrials.gov
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... An Observational Study of Patients With Primary Mitochondrial Disease (SPIMM-300). *Primary Mitochondrial Disease ... The Effect of Fibrate Therapy in Two Patients With Neutral Lipid Storage Disease With Myopathy (NLSDM). *Neutral Lipid Storage ... The Effects of Exercise Versus Inactivity on People With Mitochondrial Muscle Disease. *Mitochondrial Myopathy ...
  https://clinicaltrials.gov/search/term=Mitochondrial%20Myopathies
*  Efficacy Study of GS010 for the Treatment of Vision Loss up to 6 Months From Onset in LHON Due to the ND4 Mutation - Full Text...
Leber Hereditary Optic Atrophy. Heredity Optic Atrophy. Eye Diseases. Hereditary Eye Diseases. Inborn Genetic Disease. Genetic ... Sham Comparator: Sham-treated Eyes Each subject will have one eye randomly selected to receive GS010 and the other eye will ... Mitochondrial Disease. AAV2 Vectors. Nervous System Diseases. Neurodegenerative Disease. Heredodegenerative Disorders of the ... MedlinePlus related topics: Eye Care Genes and Gene Therapy Genetic and Rare Diseases Information Center resources: Leber ...
  https://clinicaltrials.gov/ct2/show/NCT02652767
*  Search of: Recruiting, Not yet recruiting, Available Studies | 'Blindness' - List Results - ClinicalTrials.gov
Inherited Retinal Degenerative Disease Registry. *Eye Diseases Hereditary. *Retinal Disease. *Achromatopsia. *(and 25 more...) ... Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford. *Rare Disorders ... Change in disease severity score. 150. All. Child, Adult, Senior. NCT02455414. 201301004. R01HD070855-02. TRACK. April 2012. ... Shanghai Eye Study for Older People. *Blindness,Visual Impairment, Refractive Error, Cataract, High Myopia, Aging ...
  https://clinicaltrials.gov/ct2/results?recr=Open&cond=%22Blindness%22&show_rss=Y&sel_rss=mod14
*  Trial of L-DOPA as a Treatment to Improve Vision in Albinism - Full Text View - ClinicalTrials.gov
Eye Diseases, Hereditary. Eye Diseases. Genetic Diseases, Inborn. Amino Acid Metabolism, Inborn Errors. Metabolism, Inborn ... Skin Diseases, Genetic. Hypopigmentation. Pigmentation Disorders. Skin Diseases. Metabolic Diseases. Pharmaceutical Solutions. ... Genetic and Rare Diseases Information Center resources: Albinism Inborn Amino Acid Metabolism Disorder Hypomelanotic Disorder ... Enrollment and 20 week examination will be complete eye exam with fundus photos. At weeks 5, 10, and 15, exams will include ...
  https://clinicaltrials.gov/ct2/show/NCT01176435?recr=Open&cond=%22Pigmentation+Disorders%22&rank=15
*  Key function of mutation in hereditary breast and ovarian cancer gene discovered
How incurable mitochondrial diseases strike previously unaffected families. January 15, 2018 Researchers have shown for the ... While testing genes to treat glaucoma by reducing pressure inside the eye, University of Wisconsin-Madison scientists stumbled ... Key function of mutation in hereditary breast and ovarian cancer gene discovered. September 1, 2011, Virginia Commonwealth ... first time how children can inherit a severe - potentially fatal - mitochondrial disease from a healthy mother. The study, led ...
  https://medicalxpress.com/news/2011-09-key-function-mutation-hereditary-breast.html