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15 Possible Causes for Epilepsy, Overfolded Superior Helix, Seizure

  • 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] My nephew still has giggle fits that are actually seizures.[wintermutedsun.wordpress.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] J Neurol Neurosurg Psychiatry 76: 38038383 Dening TR et al. (1988) Wilsons disease and epilepsy.[vdocuments.us]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[ncbi.nlm.nih.gov] Originally, epilepsy was reported as a feature.[ncbi.nlm.nih.gov] The patient had epileptic seizures and drop attacks only during night-time and it was not recognized during the daytime.[ncbi.nlm.nih.gov]

  • 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] Seizure 0001250 Short nose Decreased length of nose Shortened nose [ more ] 0003196 Short stature Decreased body height Small stature [ more ] 0004322 Short toe Short toes[rarediseases.info.nih.gov]

  • 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.com.pk]

  • 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] The most common seizure type seen in LKS is focal motor seizure. Focal seizures can become tonic-clonic seizures, also called bilateral convulsion.[epilepsy.com]

  • Baller-Gerold Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] This medication is used to treat epilepsy and certain psychiatric disorders.[ghr.nlm.nih.gov] She was started on carbamazepine once again and was seizure-free since then.[annalsofian.org]

  • 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] Iowa type Hereditary cerebral hemorrhage with amyloidosis, Italian type Hereditary cerebral hemorrhage with amyloidosis, Piedmont type Aldosterone-producing adenoma with seizures[csbg.cnb.csic.es] Hyperostosis, Autosomal Dominant Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus Osteosclerosis, Autosomal Dominant 144750 Genetic Test Registry Epilepsy[ukgtn.nhs.uk]

  • Chudley-McCullough Syndrome

    helix Narrow palpebral fissure Aortic aneurysm Aortic regurgitation Interrupted aortic arch Abnormality of earlobe Sandal gap Cardiomyopathy Coarse facial features Congenital[mendelian.co] Epilepsy is often found in patients with AC's and vice versa.[pediatricneurosciences.com] It is important to diagnose CMS, since typically, patients with these types of brain malformations have very substantial developmental problems and seizures; therefore it[depts.washington.edu]

  • Uncombable Hair Syndrome

    helix Short chin Myopathic facies Inverted nipples Pain insensitivity Horizontal eyebrow Oval face Overfolding of the superior helices Broad chin Micrognathia Neurological[mendelian.co] 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] Learning difficulties and seizures may occur in childhood.[mendelian.co]

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