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2,923 Possible Causes for Death in Childhood, Non-Hemolytic Unconjugated Hyperbilirubinemia, Psychomotor Development Delayed

  • Brandt Syndrome

    Icterus intermittens juvenilis; Low-grade chronic hyperbilirubinemia; Familial non-hemolytic-non-obstructive jaundice; Constitutional liver dysfunction; Unconjugated benign[] If untreated, the condition can result in death during infancy or early childhood.[] The condition is lethal and leads to the death of the child in infancy or early childhood if some medical intervention is not carried out as a therapeutic measure.[]

  • 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[] , resulting from exacerbated hemolysis) Chronic, non-immune hemolytic anemia High mean corpuscular hemoglobin concentration (MCHC) Presence of spherocytes in the peripheral[] Abstract Dravet Syndrome is a devastating childhood epilepsy disorder with high incidence of premature death plus comorbidities of ataxia, circadian rhythm disorder, impaired[]

  • Canavan Disease

    Initial Symptoms presented: • Delayed psychomotor development • Lethargy and poor head and neck control Later Symptoms Presented: • Movement Disorders • Seizures • Blindness[] Canavan disease is characterised as a rare, neurodegenerative disease that usually causes death in early childhood.[] Initial plateauing then delayed psychomotor development infantile hypotonia, lethargy, poor head & neck control 2. Later 1.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Tay-Sachs Disease

    Delay in psychomotor development. Hypotonia (followed by spasticity) Visual loss. A macular cherry-red spot.[] The classic type causes death in childhood, but some forms do not appear until adulthood and do not lead to early death.[] […] in psychomotor development, hypotonia (followed by spasticity), visual loss, and a macular cherry red spot; hexosaminidase a is deficient, leading to the accumulation of[]

    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[] , usually in childhood.[] Childhood death was mentioned. “Katie died when she was almost 2 years and four months old, which was months after we got the diagnosis.[]

    Missing: 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[] Death occurs from childhood to adult age. A milder variant, spastic paraplegia type 2 (SPG2) presents later with weakness and spasticity of the lower extremities.[] […] to mental retardation and early death.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • GM2-Gangliosidosis

    […] in psychomotor development, hypotonia (followed by spasticity), visual loss, and a macular cherry red spot; hexosaminidase a is deficient, leading to the accumulation of[] However, death in childhood is common. Symptoms in the adult form may not appear until late childhood or early adulthood.[] Clinical presentation is mainly neurological with rapidly progressive impairment (motor, cognitive and behavioral) leading to premature death, mostly in early childhood.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Neonatal Adrenoleukodystrophy

    Psychomotor development is delayed, but children are usually able to walk and say a few words.[] Childhood ALD is progressive and usually leads to total disability or death. It affects only boys because the genetic defect is sex-linked (carried on the X chromosome).[] psychomotor development.[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • 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[] Neuraminidase Deficiency Clinical Characteristics Ocular Features: A cherry red spot is may be seen in late childhood or early adolescence.[] People with typical mucolipidosis type IV have delayed development of mental and motor skills (psychomotor delay).[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Farber Disease

    […] of NP Disease as the INFANTILE FORM -- The LIVER & SPLEEN are the primary sites of lipid deposition (& are thus tremendously ENLARGED) 1)the lipid is * spingomyelin * -- Death[] […] occurs early in childhood due to damage to CNS -- Has a higher incidence in the * Ashkenazi Jew Population * than the general population -- ** FEATURES OF TYPE B ** -- Causes[]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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