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  2. 22q13 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/22q13_deletion_syndrome

    22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long arm) of chromosome 22. Any abnormal genetic variation in the q13 region that presents with significant manifestations ( phenotype ) typical of a terminal deletion may be diagnosed as 22q13 ...

  3. Phelan-McDermid syndrome - Wikipedia

    en.wikipedia.org/?title=Phelan-McDermid_syndrome&...

    This page was last edited on 22 July 2006, at 23:58 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

  4. Emergence delirium - Wikipedia

    en.wikipedia.org/wiki/Emergence_delirium

    The authors of this review were uncertain whether maintenance of anaesthesia with propofol-based total intravenous anaesthesia (TIVA) or with inhalational agents can affect incidences of postoperative delirium. [7] Emergence delirium has been associated long-term changes neurocognitive dysfunction after cardiac surgery. [8]

  5. Intellectual disability - Wikipedia

    en.wikipedia.org/wiki/Intellectual_disability

    Other genetic conditions include Phelan–McDermid syndrome (22q13del), Mowat–Wilson syndrome, genetic ciliopathy, [36] and Siderius type X-linked intellectual disability (OMIM: 300263) as caused by mutations in the PHF8 gene (OMIM: 300560). [37] [38] In the rarest of cases, abnormalities with the X or Y chromosome may also cause disability.

  6. Malignant hyperthermia - Wikipedia

    en.wikipedia.org/wiki/Malignant_hyperthermia

    Malignant hyperpyrexia, anesthesia related hyperthermia [1] Abnormalities in the ryanodine receptor 1 gene are commonly detected in people who have experienced an episode of malignant hyperthermia: Specialty: Anesthesiology, critical care medicine: Symptoms: Muscle rigidity, high body temperature, fast heart rate [1] Complications

  7. Congenital contractural arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Congenital_contractural_ar...

    Congenital contractural arachnodactyly (CCA), also known as Beals–Hecht syndrome, is a rare autosomal dominant congenital connective tissue disorder. [1] As with Marfan syndrome , people with CCA typically have an arm span that is greater than their height and very long fingers and toes . [ 2 ]

  8. Christina Applegate says MS symptoms began 6 or 7 years ... - AOL

    www.aol.com/news/christina-applegate-says-ms...

    Most people's symptoms start between the ages of 20 and 40, and the disease is three times more common in women than in men, according to the National Institutes of Health and the nonprofit ...

  9. Anesthesia awareness - Wikipedia

    en.wikipedia.org/wiki/Anesthesia_awareness

    Full wakefulness and general anesthesia are the two extremes of the spectrum. Conscious sedation and monitored anesthesia care (MAC) refer to an awareness somewhere in the middle of the spectrum, depending on the degree to which a patient is sedated. Monitored anesthesia care involves titration of local anesthesia along with sedation and ...