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

  • Pallister W Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] My nephew still has giggle fits that are actually seizures.[] […] 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[]

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

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

  • Baller-Gerold Syndrome

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

  • Kleiner Holmes Syndrome

    superior helix; Deficient auricle; Hypertelorism; Megalophthalmos; Gingival hyperplasia; Prenatal teeth; Bell-shaped thorax; Hypoplastic clavicles; Decreased mineralization[] The most common seizure type seen in LKS is focal motor seizure. Focal seizures can become tonic-clonic seizures, also called bilateral convulsion.[] Deficiency Syndrome of Myhre GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY Growth Retardation, Small and Puffy Hands and Feet, and Eczema[]

  • 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[] Most common symptoms of BRANCHIOOCULOFACIAL SYNDROME; BOFS Autosomal dominant inheritance Seizures Short stature Pica Hearing impairment More info about BRANCHIOOCULOFACIAL[] It may also be seen as a secondary infection in ear eczema (secondary impetiginization).[]

  • Chudley-McCullough Syndrome

    helix Narrow palpebral fissure Aortic aneurysm Aortic regurgitation Interrupted aortic arch Abnormality of earlobe Sandal gap Cardiomyopathy Coarse facial features Congenital[] It is important to diagnose CMS, since typically, patients with these types of brain malformations have very substantial developmental problems and seizures; therefore it[] 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[]

  • Homozygous 11p15-p14 Deletion Syndrome

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

  • 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).[] The morphology of the seizures varies from infantile spasms or focal motor seizures to generalized tonic or tonic-clonic seizures.[] […] 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[]

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