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16 Possible Causes for Epilepsy, Overfolded Superior Helix

  • Pallister W Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] What is a ‘childhood epilepsy syndrome’? If your child is diagnosed with an epilepsy syndrome, it means that their epilepsy has some specific signs and symptoms.[] According to the Epilepsy Foundation, the first seizures that present are often of the type known as gelastic (giggles) or dacrystic (crying).[]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[] Originally, epilepsy was reported as a feature.[] It is, however, commonly thought that in individuals with learning disabilities, the increased prevalence of epilepsy is related to the fact that both epilepsy and learning[]

  • Kleiner Holmes Syndrome

    superior helix; Deficient auricle; Hypertelorism; Megalophthalmos; Gingival hyperplasia; Prenatal teeth; Bell-shaped thorax; Hypoplastic clavicles; Decreased mineralization[] […] authors are internationally recognized authorities who cover everything from sleep and ADHD, headaches, restless leg syndrome, parasomnias, hypersomnias, autism, brain tumors, epilepsy[] In those children, epilepsy surgery at an epilepsy center may become an option.[]

  • Baller-Gerold Syndrome

    This medication is used to treat epilepsy and certain psychiatric disorders.[] superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] JL Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with maternal epilepsy[]

  • Propionic Acidemia

    There was mild plagiocephaly and overfolding of the superior helix of each ear. The lower lip had loss of tissue in 2 lateral clefts with bulbous tissue in the center.[] Two of them suffered from symptomatic absence epilepsy.[] […] syndrome Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency Autosomal dominant dopa-responsive dystonia Autosomal dominant myoglobinuria[]

  • Camptodactyly Syndrome Guadalajara Type 1

    Certain anti-epileptic medications increase the risk of birth defects Sudden unexplained deaths with Epilepsy: This phenomenon is not well understood, but could be related[] Dupuytren contracture has also been found in association with diabetes mellitus, epilepsy, and alcoholism.[]

  • Kaufman Oculocerebrofacial Syndrome

    Symptoms INHERITANCE: Autosomal dominant HEAD AND NECK: [Head]; Open metopic suture; [Face]; Midface hypoplasia; Micrognathia; [Ears]; Low-set ears; Overfolded superior helix[] […] lobe CHRNB2 Epilepsy, nocturnal frontal lobe CLCN2 Epilepsy, Leukoencephalopathy with ataxia DEPDC5 Epilepsy, familial focal, with variable foci EFHC1 Epilepsy, juvenile[] Epilepsy research 87 (1), 88-94 , 2009 6 2009 Function and disability in children with Costello syndrome and Cardiofaciocutaneous syndrome B Johnson, D Goldberg‐Strassler,[]

  • FGFR2-Related Bent Bone Dysplasia

    1.4 GABRD Epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to Sequencing of all coding exons of the gene - - 1.4 GABRD Generalised Epilepsy with febrile[] Hyperostosis, Autosomal Dominant Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus Osteosclerosis, Autosomal Dominant 144750 Genetic Test Registry Epilepsy[] […] exons of the gene - - 7.1 CACNB4 Episodic Ataxia - Type 2 Sequencing of all coding exons of the gene - - 1.6 CACNB4 Idiopathic generalised Epilepsy (IGE) Sequencing of all[]

  • Auriculocondylar Syndrome

    Anesthetic implications: ECG and echocardiography; epilepsy References : Diaz JH.[] Narrow mouth Overfolding of the superior helices Postauricular skin tag Posteriorly rotated ears Preauricular skin tag Round face Stenosis of the external auditory canal[] epilepsy , see juvenile myoclonic epilepsy ADPEAF , see autosomal dominant partial epilepsy with auditory features adrenal Cushing syndrome due to AIMAH , see primary macronodular[]

  • Uncombable Hair Syndrome

    Referrals are made to genetics clinics for a variety of reasons, including birth defects, developmental delay, autism, epilepsy, short stature, in the United States, physicians[] helix Short chin Myopathic facies Inverted nipples Pain insensitivity Horizontal eyebrow Oval face Overfolding of the superior helices Broad chin Micrognathia Neurological[] Broad nasal tip Long face Deeply set eye Delayed myelination Decreased fetal movement Apraxia Muscular hypotonia of the trunk Stereotypy Deep philtrum Poor head control Overfolded[]

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