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1,178 Possible Causes for Failure to Thrive in Early Infancy, Non-Hemolytic Unconjugated Hyperbilirubinemia, Psychomotor Development Delayed

  • 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: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Canavan Disease

    Initial Symptoms presented: • Delayed psychomotor development • Lethargy and poor head and neck control Later Symptoms Presented: • Movement Disorders • Seizures • Blindness[mazornet.com] infancy Lack or inability in head control Undeveloped motor skills or may lose previously acquired motor skills Failure to thrive due to difficulty in feeding and swallowing[healthool.com] Initial plateauing then delayed psychomotor development infantile hypotonia, lethargy, poor head & neck control 2. Later 1.[web.peacelink.it]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • 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]

    Missing: Failure to Thrive in Early Infancy
  • Brandt Syndrome

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

    Missing: Failure to Thrive in Early Infancy
  • Citrullinemia

    infancy. 4 71 Tomomasa T...Morikawa A 11343053 2001 12 [Failure to thrive and dyslipidemia caused by citrin deficiency: a novel clinical phenotype]. 9 38 4 Song YZ...Saheki[malacards.org] […] idiopathic neonatal hepatitis (NICCD). 38 4 8 Saheki T...Kobayashi K 12111366 2002 11 Possible clinical and histologic manifestations of adult-onset type II citrullinemia in early[malacards.org]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Neurotic Disorder

    Affected individuals may also experience delays in the acquisition of skills requiring the coordination of mental and physical activities (delayed psychomotor development)[rarediseases.org] […] or early childhood with failure to thrive, hepatosplenomegaly, and rapidly progressive neurodegenerative disorders.[orpha.net] ORPHA:77292 Classification level: Disorder Synonym(s): - Prevalence: 1 / 1 000 000 Inheritance: Autosomal recessive Age of onset: Infancy, Neonatal ICD-10: E75.2 OMIM: 257200[orpha.net]

    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[ncbi.nlm.nih.gov]

    Missing: Failure to Thrive in Early Infancy 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: Failure to Thrive in Early Infancy 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: Failure to Thrive in Early Infancy Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Zellweger Syndrome

    Bilateral cataracts are present at birth or develop soon thereafter. Seizures, profound psychomotor delays and growth failure ensue.[clinicaladvisor.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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