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657 Possible Causes for Dysautonomia, Malabsorption Syndrome

  • Autonomic Neuropathy

    We, therefore, propose a Turkish variant of familial dysautonomia in these 2 patients.[] Autonomic neuropathy is also called autonomic dysfunction or dysautonomia.[] Primary causes of autonomic neuropathy include: Familial dysautonomia (Riley-Day syndrome) Idiopathic orthostatic hypotension (progressive autonomic failure) Multiple system[]

  • Nocturnal Myoclonus Syndrome

    Syndromes Mandibulofacial Dysostosis Meniere Disease Meningism Migraine Disorders Mitral Valve Prolapse Mixed Connective Tissue Disease Movement Disorders Moyamoya Disease[] Pseudo-Obstruction Colorectal Neoplasms, Hereditary Nonpolyposis Compartment Syndromes Craniofacial Dysostosis Demyelinating Diseases Depressive Disorder Diabetic Nephropathies Vipoma Dysautonomia[] Disease Mucopolysaccharidosis I Lipoid Proteinosis of Urbach and Wiethe Hyperlipoproteinemia Type I Lymphocytic Choriomeningitis Lymphoproliferative Disorders Macular Edema Malabsorption[]

  • Beriberi

    Maintenance is recommended at 2.5-5 mg per day orally unless a malabsorption syndrome is suspected.[] Ingestion of sugar is causing widespread beriberi, masking as psychosomatic disease and dysautonomia.[] Beriberi is characterized in its early stages by dysautonomia, appearing as postural orthostatic tachycardia syndrome (POTS).[]

  • Multiple Endocrine Neoplasia Type 2B

    syndrome (two patients), and tracheal ring (one patient).[] Familial dysautonomia (FD) is a rare autosomal recessive disorder of the peripheral nervous system, affecting exclusively Jewish children of Ashkenazi extraction.[] […] misinterpretation or failure to realize the significance of one or more of these alimentary tract manifestations led to suspicion of aganglionic megacolon (three patients), malabsorption[]

  • Necrotizing Enterocolitis

    Malabsorption syndrome resulting from removal of excessive or critical portions of small Neonatal gut will grow this growth may take as long as 2 years to occur Mortality[] We present a case of a premature infant with early-onset necrotizing enterocolitis as the presenting symptom of familial dysautonomia.[] It is a malabsorption syndrome resulting from removing excessive or critical portions of the small bowel. [2] The neonatal gut typically grows and adapts over time, but this[]

  • Lactic Acidosis

    D-lactic acidosis should be considered when patients with short bowel syndrome or other malabsorption syndromes due to an altered gastrointestinal tract anatomy present with[] […] sequencing, we identified compound heterozygous RMND1 variants in a 4-year-old patient with congenital lactic acidosis, severe myopathy, hearing loss, renal failure, and dysautonomia[] ) syndromes.[]

  • Thiamine

    Syndromes in which it is difficult for the body to absorb nutrients (malabsorption syndromes) : People with malabsorption syndromes may have low levels of thiamine.[] […] the course of our research , thiamine deficiency has been observed in previously healthy, young, non-alcoholic patients, post medication or vaccine, along with symptoms of dysautonomia[] Maintenance is recommended at 2.5-5 mg per day orally unless a malabsorption syndrome is suspected.[]

  • Whipple Disease

    Differential diagnosis The differential diagnosis includes seronegative polyarthritis, ankylosing spondylitis, culture-negative endocarditis, vasculitis, malabsorption syndrome[] […] neurological signs, not due to another known etiology, as follows: Supranuclear vertical palsy Rhythmic myoclonus Dementia with psychiatric symptoms Hypothalamic manifestations (dysautonomia[] syndrome with severe weight loss, weakness and general cachexia.[]

  • Magnesium Deficiency

    Osteoporosis and magnesium (Mg) deficiency often occur in malabsorption syndromes such as gluten-sensitive enteropathy (GSE).[] It is more likely that dysautonomia, autoimmune phenomena and MVP are all manifestations of the same disturbance.[] Hypomagnesaemia This is variably defined, but usually taken as a level less than 0.7 mmol/L. [ 3 ] Aetiology [ 4 ] It may be caused by: Malabsorption syndromes, including:[]

  • Haddad Syndrome

    If the entire large intestine is removed, it will eventually lead to malabsorption syndrome, possibly short bowel syndrome also, conditions detrimental to the baby.[] […] reference - No MeSH references Very frequent - Apnea / sleep apnea - Autosomal dominant inheritance - Dolichocolon / megacolon / megadolichocolon / Hirschsprung's disease - Dysautonomia[] There is malabsorption of the amino acids tryptophan and phenylalanine.[]

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