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8,296 Possible Causes for Juvenile Familial Leg Ulcers, Large Anterior Fontanel at Birth, Seizure

  • Neonatal Adrenoleukodystrophy

    These very-early-onset seizures may require unique diagnostic and therapeutic considerations, in contrast with the later onset of seizures in neonates.[] Standard epileptic drugs are used for seizures. Lifelong follow up is needed to monitor changes in hearing, vision and liver function.[] Antepartum and peripartum seizures are very rare, and represent signs of prenatal-onset neurologic dysfunction.[]

    Missing: Juvenile Familial Leg Ulcers
  • Oculocerebrorenal Syndrome

    In monitoring the disease, the manifestation of the seizures as atonic seizures accompanied by focally initiated secondary generalized epileptic discharges is a finding previously[] Both had abnormal findings on electroencephalography and developed seizure episodes.[] A wide variability in seizure types exists, including myoclonic seizures, generalised tonic-clonic seizures, infantile spasms, and partial complex seizures.[]

    Missing: Juvenile Familial Leg Ulcers
  • Cerebral Cortical Atrophy

    Not all patients have overt seizures ( Lee et al., 2016 ).[] Seizures can take different forms, appearing as disorientation, repetitive movements, loss of consciousness, or convulsions.[] Seizure: Seizures usually occur due to the sudden occurrence of abnormal activities in the brain.[]

    Missing: Juvenile Familial Leg Ulcers
  • Citrullinemia Type 2

    Infants with Zellweger syndrome present with flattened facies, large anterior fontanel, split sutures, prominent high forehead, flattened occiput, upslanting palpebral fissures[] There are over 200 inherited disorders that are associated with seizures and prompt identification and intervention is crucial for a positive outcome.[] Characteristic features include confusion, abnormal behaviors (such as aggression, irritability, and hyperactivity), seizures, and coma.[]

    Missing: Juvenile Familial Leg Ulcers
  • Platyspondylic Lethal Skeletal Dysplasia Type San Diego

    Distinctive facial features include macrocephaly, large anterior fontanel, frontal bossing, proptosis and low nasal bridge.[] Long-term survivors need neurologic, orthopedic, and audiologic evaluations, CT to monitor for craniocervical constriction, and EEG to monitor for seizure activity.[] Rarely, cardiac and renal abnormalities have been reported as well as seizures.[]

    Missing: Juvenile Familial Leg Ulcers
  • Hydrocephalus

    It can also be used after birth while the anterior fontanelle remains open. MRI This test uses large magnets, radio waves, and a computer.[] She remained seizure-free until age five months, when seizures reappeared in the context of increasing head size and irritability.[] Overall improvement was also noted in seizures. Spasticity decrease and more cervical control were also achieved.[]

    Missing: Juvenile Familial Leg Ulcers
  • Plasmodium Falciparum Malaria

    […] bridge, widely split sutures, large anterior fontanelle), liver dysfunction, and in older children progressive sensorineural hearing loss, retinal dystrophy and developmental[] […] with seizures compared with P vivax infections in Thai children. 79 Although fever may precipitate some seizures, most seizures occur when the rectal temperatures are less[] In severe cases, it can cause jaundice, seizures, coma, or death.[]

    Missing: Juvenile Familial Leg Ulcers
  • Polycythemia Neonatorum

    Fontanelle Bulging, depressed, anterior fontanelle abnormally large ( 2x2 cm), posterior fontanelle open? HEENT Caput succadaneum?[] Newborns with polycythemia neonatorum have nonspecific findings, related most often to the central nervous and respiratory systems: irritability or lethargy, hypotonia, seizures[] Differential Diagnosis section highlights 50 new topics, including: alcohol-related seizures, dysentery and inflammatory enterocolitis, hair loss, cystic and solid pancreatic[]

    Missing: Juvenile Familial Leg Ulcers
  • Progeroid Syndrome Type Petty

    […] open anterior fontanelle, and nor- mal cognitive and motor development.[] ulcers juvenile cataracts hypogonadism, which is associated with reduced fertility tendency to develop diabetes calcification of blood vessels osteoporosis metastatic calcification[] seizure susceptibility syndrome.[]

  • Raine Syndrome

    The baby presented at birth with severe craniofacial anomalies including a wide anterior fontanelle, exophthalmos, severe depression of the nasal bridge with a hypoplastic[] Amelogenesis imperfecta, hearing loss, seizures, and intracerebral calcification are apparent in some affected individuals.[] The baby presented at birth with severe craniofacial anomalies including a wide anterior fontanel, exophthalmos, severe depression of the nasal bridge with a hypoplastic midface[]

    Missing: Juvenile Familial Leg Ulcers

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