Create issue ticket

11 Possible Causes for Eczema, Overfolded Superior Helix, Seizure

  • 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] All nine patients with pathological EEG discharges developed seizures compatible with the definition of symptomatic epilepsy.[ncbi.nlm.nih.gov] PKU)*PhenylalanineTyrosineHydroxylasePhenylalaninePhenyl ethylamine Phenyl pyruvic acid Phenylketonuria PKU*Hyperactivity, athetosis, vomiting.Blond.Seborric dermatitis or eczema[vdocuments.site]

  • Pallister W Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] My nephew still has giggle fits that are actually seizures.[wintermutedsun.wordpress.com] […] the white blood cells do not properly reach the sites of infections Without normal immune cells, a child with Wiskott-Aldrich syndrome is at constant risk for: pneumonia eczema[childrenshospital.org]

  • 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] In addition the girl suffered from atopic eczema and tooth anomalies.[unboundmedicine.com] A case report of uncombable hair in relation to atopic eczema and tooth anomalies .[eurekamag.com]

  • 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] KCNQ2 Benign familial neonatal seizures, Epileptic encephalopathy, early infantile, Myokymia KCNQ3 Seizures, benign neonatal KCNT1 Epilepsy, nocturnal frontal lobe LGI1 Epilepsy[genda.com.ar] Dubowitz syndrome 0 *Eczema *Growth Disorders *Intellectual Disability *Microcephaly *Facies.[reference.md]

  • Baller-Gerold Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] She was started on carbamazepine once again and was seizure-free since then.[annalsofian.org] After 3 months of this not improving we went to a Pediatric Dermatologist who initially treated her for eczema.[rtsplace.org]

  • Kleiner Holmes Syndrome

    superior helix; Deficient auricle; Hypertelorism; Megalophthalmos; Gingival hyperplasia; Prenatal teeth; Bell-shaped thorax; Hypoplastic clavicles; Decreased mineralization[panelapp.genomicsengland.co.uk] 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] Deficiency Syndrome of Myhre GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY Growth Retardation, Small and Puffy Hands and Feet, and Eczema[rgd.mcw.edu]

  • Branchio-Oculo-Facial Syndrome

    […] with hypoplastic superior helix, posterior and preauricular pit, supraauricular sinuses, conductive hearing loss secondary to fusion of the middle ear ossicles), the eyes[accessanesthesiology.mhmedical.com] Most common symptoms of BRANCHIOOCULOFACIAL SYNDROME; BOFS Autosomal dominant inheritance Seizures Short stature Pica Hearing impairment More info about BRANCHIOOCULOFACIAL[mendelian.co] It may also be seen as a secondary infection in ear eczema (secondary impetiginization).[otolaryngologygr.blogspot.com]

  • 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] 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] Seizure 0001250 Percent of people who have these symptoms is not available through HPO Arachnoid cyst Fluid-filled sac located in membrane surrounding brain or spinal cord[rarediseases.info.nih.gov]

  • Homozygous 11p15-p14 Deletion Syndrome

    […] fontanelle Reduced consciousness/confusion Cystinuria CNS demyelination Vegetative state Homocystinuria Decerebrate rigidity Babinski sign Hyperreflexia Relative macrocephaly Eczema[mendelian.co] […] pulmonic stenosis, septal defects, hypertrophic cardiomyopathy, arrhythmia), distinctive facial features, and cutaneous abnormalities (xerosis, hyperkeratosis, ichthyosis, eczema[quizlet.com] Rare exonic deletions implicate the synaptic organizer gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Hum Mol Genet 2013 ; 22 : 2055 – 2066. 16.[cambridge.org]

  • Tricho-Oculo-Dermo-Vertebral Syndrome

    The ears are small with overfolding of the superior part of the helix. The EACs are stenotic, especially at the isthmus (bony-cartilaginous junction).[entokey.com] The morphology of the seizures varies from infantile spasms or focal motor seizures to generalized tonic or tonic-clonic seizures.[dermaamin.com] […] individuals exhibit food allergies, in contrast to a prevalence of 6 to 8% in the general population, and LDS patients have an increased prevalence of asthma, rhinitis, and eczema[mendelian.co]

Similar symptoms