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984 Possible Causes for Generalized Bilateral Synchronous Symmetrical Discharge, Non-Hemolytic Unconjugated Hyperbilirubinemia, Psychomotor Development Delayed

  • Early Infantile Epileptic Encephalopathy Type 6

    We report on a patient who developed, from 5 months of age, multiple seizure types, including myoclonic, associated with severe psychomotor delay, leading to the diagnosis[ncbi.nlm.nih.gov] , resulting from exacerbated hemolysis) Chronic, non-immune hemolytic anemia High mean corpuscular hemoglobin concentration (MCHC) Presence of spherocytes in the peripheral[centogene.com] Over the years, he developed refractory epilepsy and was implanted with a vagus nerve stimulator at the age of 19.[ncbi.nlm.nih.gov]

  • Angelman Syndrome

    General symptoms Delayed psychomotor development. Muscle laxity and balance problems. Severe mental retardation. Epilepsy.[mun-h-center.se]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Epilepsy

    The seizures were difficult to control with antiepileptic drugs and presented some degree of psychomotor development delay.[ncbi.nlm.nih.gov]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • West Syndrome

    In this study, we report a 1.8-year-old boy, who presented with West syndrome in infancy and developed the sequelae of psychomotor delay and autism.[ncbi.nlm.nih.gov] The patient presented with West syndrome, severe psychomotor delay, failure to thrive, microcephaly, atypical ocular movements, and pyramidal signs.[ncbi.nlm.nih.gov] We created a data collection form that included the following variables: sex, age at onset, history (obstetric, personal and family), psychomotor development at onset, epileptic[analesdepediatria.org]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Brandt Syndrome

    Icterus intermittens juvenilis; Low-grade chronic hyperbilirubinemia; Familial non-hemolytic-non-obstructive jaundice; Constitutional liver dysfunction; Unconjugated benign[medlineplus.gov]

    Missing: Generalized Bilateral Synchronous Symmetrical Discharge
  • Idiopathic Generalized Epilepsy

    In idiopathic generalized epilepsy, all seizures are initially generalized with an EEG expression that is a generalized, bilateral, synchronous, symmetrical discharge.[humpath.com] SYNGAP1 gene mutations have been associated to autism spectrum disorders, delay of psychomotor development, acquired microcephaly, and several forms of idiopathic generalized[thieme-connect.com] Seizures are initially generalized with a bilateral, synchronous, generalized, symmetrical EEG discharge ({19:Zara et al., 1995}; {8:Lu and Wang, 2009}).[diseaseinfosearch.org]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Leigh's Disease

    delay – a delayed development of intellect and motor ability Dystonia – uncontrollable muscle contractions causing repetitive twisting movements Epilepsy - The condition[lhsc.on.ca] […] groups have been affected, a common mutation has been found in Faroese people (an ethnic group with a population of about 25 000 living Scandinavia) Symptoms Neurological: Psychomotor[lhsc.on.ca]

    Missing: Generalized Bilateral Synchronous Symmetrical Discharge Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Alexander Disease

    The main characteristics of infantile and juvenile AxD include delayed psychomotor development or mental retardation, convulsions, macrocephaly, and predominant cerebral white[ncbi.nlm.nih.gov]

    Missing: Generalized Bilateral Synchronous Symmetrical Discharge Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Gilbert Syndrome

    Constitutional liver dysfunction Familial non-hemolytic non-obstructive jaundice Icterus intermittens juvenilis Low-grade chronic hyperbilirubinemia Unconjugated benign bilirubinemia[en.wikipedia.org] Tagged as: constitutional liver dysfunction, familial benign unconjugated hyperbilirubinaemia, familial non-hemolytic non-obstructive jaundice, Gilbert–Meulengracht syndrome[highrisklifeinsuranceagency.com] Icterus intermittens juvenilis; Low-grade chronic hyperbilirubinemia; Familial non-hemolytic-non-obstructive jaundice; Constitutional liver dysfunction; Unconjugated benign[nlm.nih.gov]

    Missing: Generalized Bilateral Synchronous Symmetrical Discharge Psychomotor Development Delayed
  • Mucolipidosis Type 1

    Mucolipidosis IV (ML4) is a neurodegenerative condition that is characterised by significant psychomotor and cognitive development delay, visual impairment, and poor muscle[jnetics.org] People with typical mucolipidosis type IV have delayed development of mental and motor skills (psychomotor delay).[centogene.com] Case 2 also developed cerebellar syndrome with mild psychomotor delay.[healio.com]

    Missing: Generalized Bilateral Synchronous Symmetrical Discharge Non-Hemolytic Unconjugated Hyperbilirubinemia

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