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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 ).[jmg.bmj.com] 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.[epilepsysociety.org.uk] According to the Epilepsy Foundation, the first seizures that present are often of the type known as gelastic (giggles) or dacrystic (crying).[wintermutedsun.wordpress.com]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[ncbi.nlm.nih.gov] Originally, epilepsy was reported as a feature.[ncbi.nlm.nih.gov] 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[karger.com]

  • Kleiner Holmes Syndrome

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

  • Baller-Gerold Syndrome

    This medication is used to treat epilepsy and certain psychiatric disorders.[ghr.nlm.nih.gov] superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] 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[deepdyve.com]

  • 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.[jamanetwork.com] Two of them suffered from symptomatic absence epilepsy.[ncbi.nlm.nih.gov] […] syndrome Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency Autosomal dominant dopa-responsive dystonia Autosomal dominant myoglobinuria[se-atlas.de]

  • 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[dovemed.com] Dupuytren contracture has also been found in association with diabetes mellitus, epilepsy, and alcoholism.[rrnursingschool.biz]

  • 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[findzebra.com] […] lobe CHRNB2 Epilepsy, nocturnal frontal lobe CLCN2 Epilepsy, Leukoencephalopathy with ataxia DEPDC5 Epilepsy, familial focal, with variable foci EFHC1 Epilepsy, juvenile[genda.com.ar] 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,[scholar.google.it]

  • 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[cegat.de] Hyperostosis, Autosomal Dominant Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus Osteosclerosis, Autosomal Dominant 144750 Genetic Test Registry Epilepsy[ukgtn.nhs.uk] […] 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[cegat.de]

  • Auriculocondylar Syndrome

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

  • 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[wikivisually.com] helix Short chin Myopathic facies Inverted nipples Pain insensitivity Horizontal eyebrow Oval face Overfolding of the superior helices Broad chin Micrognathia Neurological[mendelian.co] 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[mendelian.co]

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