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  2. Postural orthostatic tachycardia syndrome - Wikipedia

    en.wikipedia.org/wiki/Postural_orthostatic...

    Postural orthostatic tachycardia syndrome (POTS) is a condition characterized by an abnormally large increase in heart rate upon sitting up or standing. [1] POTS is a disorder of the autonomic nervous system that can lead to a variety of symptoms, [10] including lightheadedness, brain fog, blurred vision, weakness, fatigue, headaches, heart palpitations, exercise intolerance, nausea ...

  3. What Is POTS? Explaining the Syndrome Affecting Christina ...

    www.aol.com/entertainment/pots-explaining...

    What Are Symptoms of POTS? While POTS is not life-threatening, it can be “very annoying” to those who suffer from the condition, he said. “Those people can have those dizziness episodes 20 ...

  4. Jordan's syndrome - Wikipedia

    en.wikipedia.org/wiki/Jordan's_Syndrome

    [4] [1] Patients with JS may meet some or all criteria for diagnosis with autism spectrum disorder due to many shared developmental symptoms. [3] Initial clinical findings may include macrocephaly, hypotonia, epilepsy, ophthalmologic abnormalities, and dysmorphic facial features.

  5. Orthostatic intolerance - Wikipedia

    en.wikipedia.org/wiki/Orthostatic_intolerance

    Orthostatic intolerance (OI) is the development of symptoms when standing upright that are relieved when reclining. [1] There are many types of orthostatic intolerance. OI can be a subcategory of dysautonomia, a disorder of the autonomic nervous system [2] occurring when an individual stands up. [3]

  6. Prognosis of autism - Wikipedia

    en.wikipedia.org/wiki/Prognosis_of_autism

    Most parents report that the onset of autism features appear within the first or second year of life. [ 11 ] [ 12 ] This course of development is fairly gradual, in that parents typically report concerns in development over the first two years of life and diagnosis can be made around 3–4 years of age. [ 9 ]

  7. Familial dysautonomia - Wikipedia

    en.wikipedia.org/wiki/Familial_dysautonomia

    Signs and symptoms of familial dysautonomia usually commence during infancy and worsen with age, and may include gastrointestinal dysmotility (including erratic gastric emptying, gastroesophageal reflux, abnormal esophageal peristalsis, oropharyngeal incoordination), [3] dysphagia (as poor suckling in infancy) and frequent choking/gagging, recurrent vomiting, poor weight gain [6] /growth, [7 ...

  8. AOL Mail

    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Multiple system atrophy - Wikipedia

    en.wikipedia.org/wiki/Multiple_system_atrophy

    The average lifespan after the onset of symptoms in patients with MSA is 6–10 years. [4] Approximately 60% of patients require a wheelchair within five years of onset of the motor symptoms, and few patients survive beyond 12 years. [4] The disease progresses without remission at a variable rate.