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3,984 Possible Causes for Failure to Thrive, 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[medlineplus.gov] Case1: Four-month-old male patient was admitted with diffuse skin eruptions, failure to thrive, edema, hypoalbuminemia and anemia.His sweat test was not diagnostic; but he[erj.ersjournals.com] […] to thrive Failure to thrive is also a common feature seen in acrodermatitis enteropathica. [4] Irritability Children are highly irritable.[explainmedicine.com]

  • 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] Constitutional symptoms, such as malaise, fatigue, anorexia and failure to thrive are present in many patients, while respiratory and gastrointestinal disturbances such as[symptoma.com] These problems often result in an inability to grow and gain weight at the expected rate (failure to thrive).[disabled-world.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Farber Disease

    Severe cognitive disability, failure to gain motor skills, failure to thrive, and joint contractures developed.[ncbi.nlm.nih.gov] METHODS: Here we describe a 2-year-old female, a product of a non-consanguineous Emirati union, who was quite well until 8 months of age when presented with failure to thrive[ncbi.nlm.nih.gov] Recognizable at birth or shortly after; manifests with failure to thrive, hoarse cry, feeding difficulty, irritability, motor and mental retardation and erythematous periarticular[whonamedit.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Homocystinuria

    It causes delayed psychomotor development, megaloblastic anemia, homocystinuria, and hypomethioninemia.[uniprot.org] […] to thrive, neurological abnormalities, and others depending on the cause.[medical-dictionary.thefreedictionary.com] S-adenosyl homocystine hydrolase (SAHH) deficiency similarly does not have much of an overlap phenotype except for delayed psychomotor development.[clinicaladvisor.com]

    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] The child was born after an uneventful pregnancy, presented initially only as a failure to thrive.[ncbi.nlm.nih.gov] […] to thrive, episodic deterioration, abnormal eye movements, pyramidal and cerebellar signs), urinary excretion of 3-methyl-glutaconic acid and imaging findings (extensive[ncbi.nlm.nih.gov]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Argininosuccinic Aciduria

    […] to thrive, irritability, behavioral problems or psychomotor retardation.[genedx.com] Later onset results in milder set of clinical features including vomiting, failure to thrive, irritability, behavioral problems, or psychomotor retardation.[decs.bvs.br] Common Argininosuccinate Lyase Deficiency Symptoms Lethargy, failure to thrive from birth Seizures Coma Developmental Delays Intellectual Disability Hypertension Liver enlargement[evolvegene.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Citrullinemia

    However, some patients may have a progressive course with continued failure to thrive and dyslipidemia, and a few may develop chronic or fatal liver disease.[medlink.com] Most patients present with a severe neonatal form characterized by hyperammonemia, vomiting, lethargy, failure to thrive, seizures, spasticity and increased intracranial pressure[ggc.org] In older children, citrullinemia type 2 presents with failure to thrive and dyslipidemia, but the most common presentation is in adults usually between the second and fourth[medlink.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Hartnup Disease

    Signs and symptoms[edit] Hartnup disease manifests during infancy with variable clinical presentation: failure to thrive, photosensitivity, intermittent ataxia, nystagmus,[en.wikipedia.org] A severe and untreated case of Hartnup disease that first appears in infancy may result in failure to thrive and irreversible mental retardation.[wisegeek.com] Clinical Manifestations Hartnup disease manifest during infancy with variable clinical presentation: failure to thrive, photosensitivity, intermittent ataxia, nystagmus and[namrata.co]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Neonatal Adrenoleukodystrophy

    Psychomotor development is delayed, but children are usually able to walk and say a few words.[rarediseases.info.nih.gov] Abnormal clinical features in neonatal adrenoleukodystrophy are generally present at birth, and include muscle hypotonia, severe psychomotor retardation, and failure to thrive[ncbi.nlm.nih.gov] psychomotor development.[ela-asso.com]

    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] […] to thrive Seizures : The brain controls how the body moves by sending electrical signals.[ulf.org] Initial plateauing then delayed psychomotor development infantile hypotonia, lethargy, poor head & neck control 2. Later 1.[web.peacelink.it]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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