Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 30 for Perry syndrome
  1. Perry syndrome 
    Perry syndrome is a progressive brain disease that is characterized by four major features: a pattern of movement ...
    https://medlineplus.gov/genetics/condition/perry-syndrome - Genetics
  2. DCTN1 gene 
    ... the DCTN1 gene have been found to cause Perry syndrome. This progressive brain disease is characterized by a ... breathing (hypoventilation).Most of the mutations that cause Perry syndrome change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  3. Mental Disorders (National Library of Medicine)  
    What are mental disorders? Mental disorders (or mental illnesses) are conditions that affect your thinking, feeling, mood, and behavior. They may happen ...
    https://medlineplus.gov/mentaldisorders.html - Health Topics
  4. Patient support and advocacy groups 
    ... Association Periodic Paralysis Association Periodic Paralysis International (Canada) Perry Syndrome Support Group (New Zealand) Peutz-Jehgers Syndrome & Juvenile ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  5. Movement Disorders (National Library of Medicine)  
    Movement disorders are neurologic conditions that cause problems with movement, such as: Increased movement that can be voluntary (intentional) or involuntary ( ...
    https://medlineplus.gov/movementdisorders.html - Health Topics
  6. Myhre syndrome 
    ... Delaney JW, Yetman AT, Hammel JM, Sanmann JN, Perry DA, Schaefer GB, Olney AH. Myhre syndrome: Clinical features and restrictive cardiopulmonary complications. Am J ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  7. Proximal 18q deletion syndrome 
    ... Li J, Lancaster J, Fox PT, Stratton RF, Perry B, Hale DE. Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay. Am J Med Genet ...
    https://medlineplus.gov/.../condition/proximal-18q-deletion-syndrome - Genetics
  8. MT-TL1 gene 
    ... RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1 SUDDEN INFANT DEATH SYNDROME NCBI Gene ClinVar Betts J, Jaros E, Perry RH, Schaefer AM, Taylor RW, Abdel-All Z, ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  9. What is Prader-Willi Syndrome? (Prader-Willi Syndrome Association)  
    Prader-Willi Syndrome/Learn More ... Prader-Willi Syndrome ... Learn about Prader-Willi Syndrome, its symptoms, causes, and key facts about this rare genetic disorder. ...
    https://www.pwsausa.org/what-is-prader-willi-syndrome - External Health Links
  10. Trichohepatoenteric syndrome 
    ... J, Marinier E, Martinez-Vinson C, Peretti N, Perry A, Roquelaure B, Venaille A, Sarles J, Goulet O, Badens C. Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child. 2014 Jan;99(1):35- ...
    https://medlineplus.gov/.../condition/trichohepatoenteric-syndrome - Genetics
previous · 1 · 2 · 3 · next