angelman syndrome adults - Search
  1. Also known as: happy puppet syndrome
    Content medically reviewed by
    Dr. Rakshith Bharadwajverified specialist
    MD, Internal Medicine
    View full profile onLinkedIn logoLinkedIn
    Prevention

    This condition cannot be prevented. But if there is a family history, it is recommended to get genetic counseling before pregnancy.

    Symptoms & Reports
    If you are experiencing new, severe, or persistent symptoms, contact a health care provider.

    The symptoms include:

    • Impaired speech
    • Ataxia
    • Scoliosis- curvature of the spinal cord
    • Happy and excitable
    • Seizures and convulsions beginning at age 2
    • Have reduced sleeping time compared to other children
    • Short attention span
    • Frequently sticking out the tongue
    • Hair, skin, eyes are pale


    Common symptoms and their severity as reported by people on Patientslikeme.

    Symptoms
    Severity Graph
    (11)
    (10)
    (10)
    (10)
    Last Update : 2024-04-01.
    Seve...
    Mode...
    Mild
    None
    Causes

    • The condition is caused by loss of function of UBE3A gene
    • This can result from mutation or deletion of the gene.
    • It may also occur as a result of inactivation of the gene due to other chromosomal changes.
    • In rare cases, a child may inherit two copies of inactive forms of the gene instead of one active and one inactive (uniparental disomy).

    Complications

    If untreated for a prolonged period it may lead to

    • Feeding difficulties
    • Abnormal sleep-wake patterns
    • Scoliosis
    • Obesity due to large appetite

    Source: Focus Medica . For informational purposes only. Consult a medical professional for advice. Learn more

    People also ask

    How common is Angelman syndrome?
    The prevalence of Angelman syndrome is estimated to be approximately 1 in 12,000-20,000 people in the general population. However, many cases may go undiagnosed making it difficult to determine the disorder’s prevalence in the general population. Symptoms of the following disorders can be similar to those of Angelman syndrome.
    rarediseases.org/rare-diseases/angelman-syndrome/
    Are gigantism and acromegaly 100% genetic diseases?
    No, gigantism and acromegaly are not 100% genetic as there can be several other causes leading to these growth disorders most common among which is hypo or hyper secretion of the growth hormone from the pituitary.
    microsoftstart.msn.com/en-us/health/ask-professionals/i…
    What are the symptoms of Angelman syndrome?
    Angelman syndrome symptoms include: Developmental delays, including no crawling or babbling at 6 to 12 months. Mental disability, also called intellectual disability. No speech or little speech. Trouble walking, moving or balancing. Smiling and laughing often and seeming happy. Being easy to excite. Trouble sucking or feeding.
    www.mayoclinic.org/diseases-conditions/angelman-syndr…
    Is Angelman syndrome a progressive disease?
    Despite these limitations, Angelman syndrome is not a progressive disease. Therefore, with ongoing physical, occupational, and communication therapy, individuals with the disorder may be able to learn to dress, eat with a knife and fork, respond to basic instructions, and perform household chores.
    www.verywellhealth.com/angelman-syndrome-overview-4…
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  2. Angelman syndrome - Symptoms and causes - Mayo Clinic

     
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  13. Symptoms, Causes, and Treatments of Angelman Syndrome

  14. What is Angelman Syndrome – Angelman Syndrome Foundation

  15. Angelman syndrome in adulthood - Larson - Wiley Online Library

  16. Clinical aspects of a large group of adults with Angelman syndrome

  17. Angelman Syndrome - StatPearls - NCBI Bookshelf

    WebNov 9, 2020 · Angelman syndrome is a rare disorder caused by loss of function of the maternal UBE3A. It presents in childhood with psychomotor delay, absent speech, ataxia, and motor impairments. This activity …

  18. Angelman syndrome - NHS

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  22. Angelman Syndrome - GeneReviews® - NCBI Bookshelf

    WebSep 15, 1998 · Angelman syndrome (AS) is characterized by severe developmental delay or intellectual disability, severe speech impairment, gait ataxia and/or tremulousness of the limbs, and unique behavior with …

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