Results 1 - 10 of 15 for Usher "syndrome," type 1
  1. Usher Syndrome From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    ... are the characteristics of the three types of Usher syndrome? Type 1 Children with type 1 Usher syndrome are profoundly deaf at birth and have severe ...
  2. Variant of Usher Syndrome Gene Preserves Vision and Balance From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    ... mutations and lead to Usher syndrome. People with Usher syndrome type 1 are born profoundly deaf, have balance problems, and ... aware that some versions of this gene cause Usher syndrome type 1. To explain the potential outcomes, genetic counseling should ...
  3. Genetics Home Reference: Usher syndrome From the National Institutes of Health (National Library of Medicine)  
    ... Registry: Retinitis pigmentosa-deafness syndrome Genetic Testing Registry: Usher syndrome, type 1 Genetic Testing Registry: Usher syndrome, type 1C Genetic ...
  4. ... Throat Disorders Thyroid Cancer Tinnitus Tonsils and Adenoids Usher Syndrome ... Type 1 Diabetes Type 2 Diabetic Diet Diabetic Eye Problems ...
  5. Bloom's Syndrome (Chicago Center for Jewish Genetic Disorders)  
    ... Type A Spinal Muscular Atrophy Tay-Sachs Disease Usher Syndrome, Type 1F and Type III Walker-Warburg Syndrome Hereditary Cancer Others Sephardic Genetic Traits Cancer Genetics Personal Story Bloom’s Syndrome Quick Facts Disease Frequency: 1 in 50,000 in the Ashkenazi Jewish population ...
  6. Pediatric Vestibular Disorders (Vestibular Disorders Association)  
    ... otitis media 10,11 Congenital sensorineural hearing loss 1,12,13,14 ... as Usher syndrome-type I (with severe profound sensorineural hearing loss and ...
  7. Living with Hearing and Vision Loss Due to Usher Syndrome Video (American Foundation for the Blind)  
    ... Living with Hearing and Vision Loss Due to Usher Syndrome Video NARRATOR 1: A woman with short gray hair. NARRATOR 2: Mary Peck has Usher Syndrome. In this series of videos, she tells her ...
  8. G6PD Deficiency (Chicago Center for Jewish Genetic Disorders)  
    ... Familial Mediterranean Fever G6PD Deficiency Glycogen Storage Disease, Type III Wolman Disease Cancer Genetics Personal Story G6PD Deficiency Quick Facts Disease Frequency: 400 million people worldwide Carrier Frequency: 1 in 4 to1 in 20 in tropical Africa, ...
  9. Genetics Home Reference: Retinitis pigmentosa From the National Institutes of Health (National Library of Medicine)  
    ... ataxia, and retinitis pigmentosa (NARP). Read more about Usher syndrome ; Refsum disease ; neuropathy, ataxia, and retinitis pigmentosa ; and Bardet-Biedl syndrome . How common is retinitis pigmentosa? Retinitis pigmentosa is one of the most common inherited diseases of the ...
  10. Chicago Center for Jewish Genetic Disorders (Chicago Center for Jewish Genetic Disorders)  
    Advocate Genetics Webinar Series Integrating Genetics Into Your Practice Learn More Genetic education & screening now ON DEMAND! The Center's subsidized program ...
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