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501 Possible Causes for Coarse Facial Features, Coronary Artery Disease, Seizure

  • Fabry Disease

    , ventricular tachycardia, atrial fibrillation and coronary artery disease).[] Often patients have slight builds with characteristic coarse facial features and delayed puberty.[] Patients may present with transient ischemic attacks, vascular thromboses, seizures, or hemorrhagic or ischemic stroke.[]

  • Chronic Alcoholism

    […] hypertension Apoplexy Coronary heart disease Metabolism : Hypertriglyceridemia Hyperuricemia Hypoglycemia Porphyria cutanea tarda Hyperchromic anemia in folic acid deficiency[] Report of a case of SESA syndrome: a rare CNS complication of chronic alcoholism, known since 1981 and characterized by epileptic seizures, multiple and reversible neurological[] The first had been admitted with confusion and weight loss, the second with hypotension and sepsis, and the third with confusion and hypoglycaemia-induced seizures.[]

  • Mucopolysaccharidosis

    Severe coronary artery disease is well recognized in severe type I mucopolysaccharidosis (Hurler syndrome), but unexpected coronary artery disease occurs in other, "non-Hurler[] facial features, developmental delay, and an elevated quantitative urine glycosaminoglycan (GAG) level.[] However, a clear association between EEG, CNS and the history of seizures was not established.[]

  • Mucopolysaccharidosis 2

    A thickened myocardium eventually leads to coronary artery compromise, myocardial disease, and, in conjunction with airway disease, pulmonary hypertension.[] Other symptoms may include carpal tunnel syndrome, coarse facial features, deafness, hairy body (hypertrichosis), joint stiffness, and a large head (macrocephaly).[] In addition, both had features not commonly seen in this disorder, e.g. early onset of seizures in one patient and ptosis in the other.[]

  • Aspartylglucosaminuria

    For Cardiovascular Group: Either have coronary artery disease, rhythm or conduction abnormality, cardiomyopathy or valvular disease.[] facial features, and skeletal abnormalities become evident by adolescence.[] An analysis of 121 Finnish patients showed that 22 to 78 adults (28%) and one of 43 children (2%) had epileptic seizures.[]

  • Atkin Syndrome

    Insulin resistance-related factors, but not glycemia, predict coronary artery disease in type 1 diabetes: 10 year follow-up data from the Pittsburg Epidemiology of Diabetes[] Abstract We report two sisters with mental retardation, coarse facial features, telecanthus, flat malar region, prominent lower lip, kyphoscoliosis, and tapering fingers.[] seizures (n 14), atypical absence seizures (n 5), and tonic seizures (n 2).[]

  • Pallister W Syndrome

    The identification of Syndrome W before the onset of overt impaired glucose tolerance, diabetes, or manifestations of coronary artery disease could have important clinical[] facial features as child gets older, broad nasal bridge, streaks or patches of lighter or darker skin, sparse hair or bald patches, high arched or cleft palate, shorter arms[] My nephew still has giggle fits that are actually seizures.[]

  • Juvenile Myxedema

    Hyperlipidemia Coronary artery disease Hypertension Neonatal/congenital hypothyroidism Prolonged jaundice Hoarse cry Constipation Somnolence Feeding problems Impaired mental[] Seizures have been reported rarely in association with the initiation of levothyroxine sodium therapy and may be related to the effect of thyroid hormone on seizure threshold[] In elderly patients with history of coronary artery disease the full replacement dose should not be immediately administered.[]

  • Metabolic Disease

    Abstract The pathophysiology of metabolic diseases such as coronary artery disease, diabetes, and obesity is complex and multifactorial.[] Pale, yellow skin; loss of the outer edge of the eyebrows; thin and brittle hair; coarse facial features; brittle nails; firm swelling of the arms and legs; and mental slowing[] A 4-month-old female baby visited an outpatient clinic due to poor weight gain, repeated seizure-like episodes, developmental delay, and unexplained hepatomegaly with abnormal[]

  • Costello Syndrome

    The most likely diagnosis is: a) Coronary artery disease b) Dilated cardiomyopathy c) Hypertrophic cardiomyopathy 3) In this paper not much detailed information is given about[] facial features and skeletal and cardiac abnormalities.[] Central nervous system involvement includes developmental delay and seizure disorders while endocrine abnormalities have been reported including hypothalamic-pituitary dysfunction[]

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