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esthetical    
a. 美的;富美感的;美学的

美的;富美感的;美学的

esthetical
adj 1: concerning or characterized by an appreciation of beauty
or good taste; "the aesthetic faculties"; "an aesthetic
person"; "aesthetic feeling"; "the illustrations made the
book an aesthetic success" [synonym: {aesthetic}, {esthetic},
{aesthetical}, {esthetical}] [ant: {inaesthetic},
{unaesthetic}]


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  • SCN8A Treatments: Balancing Seizure Control Quality of Life
    IMPORTANT: While this consensus data provides new and valuable insights about best practices in the diagnosis and treatment of SCN8A, this is not medical advice It can inform clinicians and caregivers alike in developing optimal treatment plans for each individual
  • Home - The Cute Syndrome Foundation
    SCN8A is a rare disorder, caused by a genetic variation in the gene SCN8A Early stages of diagnosis and understanding have revealed a broad spectrum of neurodevelopmental disorders ranging from mild behavior or movement disorders to severe developmental and cognitive delays
  • About SCN8A - The Cute Syndrome Foundation: SCN8A Support . . .
    SCN8A is a rare disorder that causes a range of symptoms that can include severe epilepsy, developmental delay, and other medical challenges Every person with this condition is affected differently and with varying severity
  • SCN8A-Related Epilepsy - Childrens Hospital of Philadelphia
    In some cases, the pathogenic SCN8A variant has been inherited from a parent who also has a history of seizures A family history of epilepsy may suggest an inherited SCN8A variant In rare cases, the pathogenic SCN8A variant has been passed on from an asymptomatic parent due to parental mosaicism Just like a mosaic piece of art, in which each
  • Rare Disease Day - SCN8A Alliance
    Rare disease day is celebrated on the last day of February every year It is a day to raise awareness of the roughly 7000 rare diseases that affect over 300 million people around the world SCN8A isn’t just rare, it is ultra rare With roughly 800 people identified worldwide to date, this is an extremely rare disorder
  • 5 Questions Answered About Rare SCN8A-related Epilepsy
    February 9 marks SNC8A Awareness Day worldwide A rare cause of refractory epilepsy, SCN8A mutations have now been described in over 250 patients worldwide and several receive their care at Cook Children’s To raise awareness of this rare genetic cause of epilepsy, Dr M Scott Perry MD, Medical Director of Neurology and Director of the Genetic
  • Home - SCN8A Alliance
    Through our tireless efforts to bring awareness to SCN8A and other rare epilepsies we helped form and run the Epilepsies Action Network, working to raise awareness of and funding for the rare epilepsies
  • SCN8A FAQ : Understanding the Spectrum Disorder - SCN8A Alliance
    SCN8A epilepsy is a a rare syndrome that often manifests in difficult to treat epilepsy beginning in early life and significantly impacting development and quality of life We are learning that there are many different forms of SCN8A that lead to different kinds of seizures, levels of development and response to medications





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