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628 Possible Causes for Average Intelligence, Mutation in the Thyroid Hormone Receptor Interactor 11 Gene

  • Achondrogenesis

    In mice, a nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), resulted in[en.wikipedia.org] A nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), showed defects that[symptoma.com]

  • Parkinson's Disease

    Oral surgery can be difficult in patients with chorea-like dyskinesia, which is common in those on long-term levodopa medication for Parkinson's disease, and we know of no conclusive evidence to indicate whether conscious sedation with midazolam is effective in such cases. We report a patient in whom levodopa-induced[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Rolandic Epilepsy

    Tiziana Zilli, Sergio Zanini, Stefania Conte, Renato Borgatti and Cosimo Urgesi, Neuropsychological assessment of children with epilepsy and average intelligence using NEPSY[doi.org] RESULT: the obtained data indicate that although intellectual efficiency (measured through the Intelligence Quatient - IQ) was within average, children with rolandic epilepsy[ncbi.nlm.nih.gov] Learning disability: An abnormal condition affecting children of normal or above-average intelligence, characterized by difficulty in learning fundamentals such as reading[childneurologyfoundation.org]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Mucopolysaccharidosis

    Morquio A presents average intelligence, and MPS type VI points to deficits partially related to sensory impairment, implying significant differences between them.[lifescienceglobal.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Syringomyelia

    A 20-year-old male presented with neck pain and motor impairment of the upper extremities because of recurrent syringomyelia caused by ventriculoperitoneal shunt malfunction. A computed tomography scan after shuntgraphy demonstrated opacity in the intracranial ventricular system and cervical syrinx with[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Amyotrophic Lateral Sclerosis

    Article Access Statistics Viewed 5646 Printed 153 Emailed 3 PDF Downloaded 132 Comments power in amyotrophic lateral sclerosis patients: A study of alpha activity in an awake relaxed state 1 Centre for Biomedical Engineering, Indian Institute of Technology, Delhi, Hauz Khas, New Delhi - 110 016, India 2 Department of[…][neurologyindia.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Motor Neuron Disease

    Motor neuron disease (MND) is occasionally aggravated by chronic infection. A misdiagnosed case of tuberculosis with MND is illustrated in a 45-year-old woman who underwent successful VATS wedge excision, which is presented herein. MND in an adult is a rare clinical entity. In order to facilitate the preoperative[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Hallermann-Streiff Syndrome

    The average final height for females is about 60 in (152 cm) and for males it is about 61 in (155 cm).[encyclopedia.com] Most individuals are of normal intelligence; however, it is estimated that 15-30% of individuals with Hallermann-Streiff syndrome show some degree of mental impairment or[encyclopedia.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Chorea Gravidarum

    Chorea gravidarum is a term denoting the appearance of non-voluntary, non-rhythmic and abrupt movements during pregnancy, often without an identifiable cause. Antiphospholipid syndrome, rheumatic fever, and use of oral contraceptives are considered as most important conditions that can induce chorea gravidarum[…][symptoma.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Movement Disorder

    Neuroacanthocytosis is a genetic neurodegenerative disorder with syndromes of variable inheritance. These hyperkinetic movement disorders are reported to be very rare. It is associated with choreiform movements, orofacial and lingual dyskinesias and acanthocytes on peripheral smear and normolipoproteinemia. Here[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene

Further symptoms