Create issue ticket

13 Possible Causes for Overfolded Superior Helix, Poor Feeding, 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.[] A new case of propionic acidemia is presented, paying special attention to the early symptoms of this disease, such as increased drowsiness, muscular hypotonia, poor feeding[] All nine patients with pathological EEG discharges developed seizures compatible with the definition of symptomatic epilepsy.[]

  • Pallister W Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] Clinical diagnosis is based on a variety of characteristics common to Williams syndrome, including the typical facial features, heart problems, poor feeding and developmental[] My nephew still has giggle fits that are actually seizures.[]

  • 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[] difficulties Feeding problems Poor feeding [ more ] 0011968 Growth delay Delayed growth Growth deficiency Growth failure Growth retardation Poor growth Retarded growth [[] KCNQ2 Benign familial neonatal seizures, Epileptic encephalopathy, early infantile, Myokymia KCNQ3 Seizures, benign neonatal KCNT1 Epilepsy, nocturnal frontal lobe LGI1 Epilepsy[]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[] Sucking/feeding difficulties, poor growth, ophthalmologic abnormalities, hearing impairment, and spinal anomalies are common findings.[] […] sound-startle, a predominantly hypertonic reaction varying from hyperekplexia to a more prolonged tonic reaction resembling startle epilepsy, and true unprovoked epileptic seizures[]

  • Camptodactyly Syndrome Guadalajara Type 1

    Learn more about how to achieve it with Mendelian Learn more Other signs and symptoms that you may find interesting Feeding difficulties and Type I diabetes mellitus, related[] […] can lead to fall injuries affecting the head, or cause bone fractures Status Epilepticus is a seizure that lasts longer than normal.[] 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[]

  • Baller-Gerold Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[] Common finding in infantile GM1 gangliosidosis are cardiomyopathy, seizures, hepatosplenomegaly and poor feeding.[] She was started on carbamazepine once again and was seizure-free since then.[]

  • Homozygous 11p15-p14 Deletion Syndrome

    helix Central apnea Ankylosis Upper airway obstruction Long penis Neurodevelopmental delay Poroma Snoring Overfolding of the superior helices Speech articulation difficulties[] difficulties in infancy Vomiting Abnormality of the digestive system Diarrhea Feeding difficulties in infancy Vomiting Abnormality of the endocrine system ... ...[] Feeding difficulties in infancy MedGen UID: 436211 • Concept ID: C2674608 • Finding Impaired feeding performance of an infant as manifested by difficulties such as weak and[]

  • Kleiner Holmes Syndrome

    superior helix; Deficient auricle; Hypertelorism; Megalophthalmos; Gingival hyperplasia; Prenatal teeth; Bell-shaped thorax; Hypoplastic clavicles; Decreased mineralization[] SQUAMOUS CELL CARCINOMA OF THE ESOPHAGUS Is also known as escc; esophageal epidermoid carcinoma; esophageal squamous cell carcinoma Related symptoms: Feeding difficulties[] The most common seizure type seen in LKS is focal motor seizure. Focal seizures can become tonic-clonic seizures, also called bilateral convulsion.[]

  • 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[]

  • Verloove-Van Horick-Brubakk Syndrome

    helix Overfolding of the superior helices Impaired mastication Atresia of the external auditory canal External ear malformation Abnormality of the outer ear Poroma Aplasia[] Learning difficulties and seizures may occur in childhood.[] 3862 Microcephaly, primary autosomal recessive 3863 Microcephaly, seizures, and developmental delay 3864 Microcephaly-albinism-digital anomalies syndrome 3865 Microcephaly-cardiomyopathy[]

Similar symptoms