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  2. GLUT1 deficiency - Wikipedia

    en.wikipedia.org/wiki/GLUT1_deficiency

    GLUT1 deficiency is characterized by an array of signs and symptoms including mental and motor developmental delays, infantile seizures refractory to anticonvulsants, ataxia, dystonia, dysarthria, opsoclonus, spasticity, other paroxysmal neurologic phenomena and sometimes deceleration of head growth also known as microcephaly. The presence and ...

  3. GLUT1 - Wikipedia

    en.wikipedia.org/wiki/GLUT1

    Mutations in the GLUT1 gene are responsible for GLUT1 deficiency or De Vivo disease, which is a rare autosomal dominant disorder. [14] This disease is characterized by a low cerebrospinal fluid glucose concentration (hypoglycorrhachia), a type of neuroglycopenia, which results from impaired glucose transport across the blood–brain barrier.

  4. Hypothyroidism in dogs - Wikipedia

    en.wikipedia.org/wiki/Hypothyroidism_in_dogs

    Thyrotoxicosis is a rare side effect in dogs receiving levothyroxine treatment due to the half-life and poor absorption. Thyrotoxicosis occurs when a dog is either given too much levothyroxine or has issues with metabolising it. Symptoms include: polypynoea, anxiety, tachycardia, aggression, polyuria, polydipsia, polyphagia, and cachexia. [2]

  5. Canine degenerative myelopathy - Wikipedia

    en.wikipedia.org/wiki/Canine_degenerative_myelopathy

    A dog with degenerative myelopathy often stands with its legs close together and may not correct an unusual foot position due to a lack of conscious proprioception. Canine degenerative myelopathy, also known as chronic degenerative radiculomyelopathy, is an incurable, progressive disease of the canine spinal cord that is similar in many ways to amyotrophic lateral sclerosis (ALS).

  6. Paroxysmal dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Paroxysmal_dyskinesia

    The different subtypes make accurate and quick diagnosis of PD challenging. Thus, PD is often under reported and misdiagnosed, making it difficult to accurately study its prevalence in human populations. Onset of PD is usually in late childhood to early adolescence. New drug regimens help treat symptoms of PD, but no cure for the disorder is known.

  7. White dog shaker syndrome - Wikipedia

    en.wikipedia.org/wiki/White_dog_shaker_syndrome

    One theory is that there is an autoimmune-induced generalized deficiency of neurotransmitters. [2] Cerebrospinal fluid analysis may reveal an increased number of lymphocytes. [3] Treatment with corticosteroids may put the dog into remission, or diazepam may control the symptoms. [4] Typically the two drugs are used together. [5]

  8. ‘12 Badass Women’ by Huffington Post

    testkitchen.huffingtonpost.com/badass-women/?ir=...

    The Huffington Post reached out to historians across the country to create a list of women who deserve more recognition for their accomplishments.

  9. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Signs and symptoms [ edit ] Because of the enormous number of these diseases and the numerous systems negatively impacted, nearly every "presenting complaint" to a healthcare provider may have a congenital metabolic disease as a possible cause, especially in childhood and adolescence.