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14 Possible Causes for High-Arched Palate (61%), Paroxysmal Activity - Sharp-Waves Temporal Right

Did you mean: High-Arched Palate (61, ), Paroxysmal Activity - Sharp-Waves Temporal Right

  • Fragile X Syndrome

    The most frequent findings were inner canthal distance 3.5 cm (100%), macro-orchidism (81%), long and narrow face (77%), high arched palate (70%), avoidance of eye contact[scielo.br] (61%), prominent ears (54%), large ears (46%), hand calluses (38%) and hyperactivity (38%).[scielo.br]

  • Epilepsy

    Contemporary drug therapy fails to control epileptic seizures in some 30% of patients, resulting in the need to employ other measures when they appear practicable. A good deal of potentially relevant statistical detail is available regarding the outcomes of the available antiepileptic therapies, but its interpretation[…][ncbi.nlm.nih.gov]

    Missing: High-Arched Palate (61%)
  • Vascular Dementia

    Many of the previous studies of vascular dementia using proton magnetic resonance (MR) spectroscopy had been carried out on white matter. However, no proton spectroscopic data of the subcortical gray matter are available in such disease. We report two cases suffering from vascular dementia, with an unilateral[…][ncbi.nlm.nih.gov]

    Missing: High-Arched Palate (61%)
  • Encephalitis

    Rev Neurol (Paris). 2018 Apr;174(4):228-236. doi: 10.1016/j.neurol.2017.11.004. Epub 2018 Mar 31. Author information 1 Centre de référence maladies rares 'Syndromes neurologiques paranéoplasiques', hospices civils de Lyon, hôpital neurologique, neurologie B, 69677 Bron, France; INMG (NeuroMyoGene Institut), Inserm U1217/CNRS[…][ncbi.nlm.nih.gov]

    Missing: High-Arched Palate (61%)
  • Rolandic Epilepsy

    Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood. Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14–18), hence the label benign. The seizures,[…][en.wikipedia.org]

    Missing: High-Arched Palate (61%)
  • Creutzfeldt Jakob Disease

    […] degenerative neurological disorder CJD CJD (Creutzfeldt Jakob disease) Creutzfeldt Jacob syndrome Creutzfeldt Jakob disease Creutzfeldt-Jacob disease Jakob-Creutzfeldt disease Subacute spongiform encephalopathy Transmissible virus dementia (disorder) Transmissible virus dementia Classic Creutzfeldt-Jakob Disease[…][wikidata.org]

    Missing: High-Arched Palate (61%)
  • Periventricular Leukomalacia

    Hemorrhage into areas of periventricular leukomalacia may occur and range in size from microscopic to massive. Hitherto, the definitive diagnosis has been made only at autopsy. A case is described in which the diagnosis of hemorrhagic periventricular leukomalacia was made antemortem by real-time ultrasound scanning[…][ncbi.nlm.nih.gov]

    Missing: High-Arched Palate (61%)
  • Moebius Syndrome

    palate (61%) tongue hypoplasia (77%), teeth defects (37%) Limb malformations Syndactyly, oligodactyly, brachydactyly, arthrogryposis, absent trapezius or pectoral muscles[patient.info] 2 ] Associated abnormalities [ 1 ] Orofacial dysmorphism Micrognathia (64% of patients), ocular hypertelorism (25%), epicanthal folds (89%), external ear defects (47%), high-arched[patient.info]

    Missing: Paroxysmal Activity - Sharp-Waves Temporal Right
  • Zellweger Syndrome

    palate 50% (4/8) 95% (35/37) present abnormal ears 50% (4/8) 98% (39/40) present high forehead present 97% (58/60) present neonatal seizures no 92% (56/61) 95% (36/38) neuronal[dx.doi.org] […] mental retardation 86% (6/7) 100% (45/45) yes short upturned nose with low nasal bridge 75% (6/8) 100% (23/23) present micrognathia 63% (5/8) 100% (18/18) present Highly arched[dx.doi.org]

    Missing: Paroxysmal Activity - Sharp-Waves Temporal Right
  • Mandibuloacral Dysostosis

    Intraorally multiple retained deciduous teeth were present and 51, 54, 61 and 85 were carious. High arched palate.[jiaomr.in]

    Missing: Paroxysmal Activity - Sharp-Waves Temporal Right

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