Create issue ticket

43 Possible Causes for Hyperbilirubinemia, Onset in First Weeks or Months of Life, Pediatric Disorder

  • Neonatal Sepsis

    Early-onset sepsis is seen in the first week of life. Occurs after 1 week and before 3 months of age.[omicsonline.org] Data Cues list assessment data to help you recognize possible pediatric disorders.[books.google.com] The incidence rate of hyperbilirubinemia due to infection is unknown (7,8).[ijp.mums.ac.ir]

  • Hemorrhagic Disease of the Newborn

    […] gestational age infant (LGA) Physical maturity Pathology of prematurity Gross appearance of premature infant Difficulties in maintaining homeostasis Thermoregulation Hypoglycemia Hyperbilirubinemia[atlases.muni.cz] It usually occurs from the second day of life to the end of the first week; however, it can occur during first month and sometimes overlaps with late-onset vitamin K deficiency[emedicine.com] disorders, are treated through our Pediatric Hematology service.[childrenshospital.org]

  • Cholestasis

    Clinical description The first cholestatic episode can occur at any age but onset within the first two decades of life is most common.[orpha.net] […] of the biliary tract gallstones acute hepatitis cystic fibrosis intrahepatic cholestasis of pregnancy (obstetric cholestasis) primary biliary cholangitis, an autoimmune disorder[en.wikipedia.org] We believe our patient’s persistent direct hyperbilirubinemia with biopsy-confirmed cholestasis was also likely related to his AHC.[pediatrics.aappublications.org]

  • Neonatal Infection

    Early-onset sepsis is seen in the first week of life. Late onset sepsis occurs after 1 week through 3 months of age.[nlm.nih.gov] Significance of serial C-reactive protein responses in neonatal infection and other disorders. Pediatrics 1993 ; 92 : 431 -435.[clinchem.aaccjnls.org] […] low-risk for having a serious bacterial illness: [2] generally well-appearing previously healthy full term (at 37 weeks gestation) no antibiotics perinatally no unexplained hyperbilirubinemia[en.wikipedia.org]

  • Wolman Disease

    This particular form of these disorders is early in onset, usually developing within the first weeks or month of life.[disability-benefits-help.org] […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[books.google.de] Significant hyperbilirubinemia (peak total and direct bilirubin levels: 54.4 and 45.8 mg/dl, respectively) developed at 7 weeks from BMT.[nature.com]

  • Glycogen Storage Disease Type 2

    Deletion Syndrome, Adrenoleukodystrophy, Critical Congenital Heart Disease, Fabry Disease, Hemoglobin H, Krabbe Disease, MPS 1 (alpha-L-idurinidase deficiency), Neonatal Hyperbilirubinemia[us5.campaign-archive1.com] Infantile GSDII presents during the first weeks or months of life with poor feeding, failure to thrive, macroglossia, severe hypotonia, cardiomegaly, mild hepatomegaly, and[genedx.com] Nomenclature for Conditions based upon “Naming and Counting Disorders (Conditions) Included in Newborn Screening Panels.” Pediatrics. 2006; 117 (5) Suppl: S308-S314.[hrsa.gov]

  • Glycogen Storage Disease

    Infantile GSDII presents during the first weeks or months of life with poor feeding, failure to thrive, macroglossia, severe hypotonia, cardiomegaly, mild hepatomegaly, and[genedx.com] Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of Gluconeogenesis. Pediatr Clin North Am. 2018 Apr. 65 (2):247-265.[emedicine.medscape.com] […] fixed myopathy in some patients Systemic features Gout: Hyperuricemia Gastric ulcer Laboratory Serum CK During episodes: High Between episodes: Often normal Hyperuricemia Hyperbilirubinemia[neuromuscular.wustl.edu]

  • Beckwith-Wiedemann Syndrome

    Occasionally, onset of hypoglycemia is delayed until the first month after birth.[encyclopedia.com] Beckwith-Wiedemann syndrome (BWS) is a pediatric overgrowth disorder involving a predisposition to tumor development, including adrenal lesions.[ncbi.nlm.nih.gov] After birth the infant became plethoric and presented with unconjugated hyperbilirubinemia, for which she received phototherapy.[pediatrics.aappublications.org]

  • Sclerema Neonatorum

    .); Liver Function Analysis on Unconjugated Hyperbilirubinemia of 100 newborn [A];[C];2009 4 XU Xiao-Hua HUANG Guo-Ying CHEN Chao CAO Yun.[en.cnki.com.cn] SN is typically seen in the first few days after birth but may develop as late as several weeks of life 1.[synapse.koreamed.org] Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.com]

  • Intrahepatic Cholestasis

    Dubin-Johnson syndrome may manifest as conjugated hyperbilirubinemia, darkly pigmented liver, presence of abnormal pigment in the parenchyma of hepatocytes and abnormal distribution[ncbi.nlm.nih.gov] Clinical description The first cholestatic episode can occur at any age but onset within the first two decades of life is most common.[orpha.net] Pediatric Surgery and Transplantation, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.[ncbi.nlm.nih.gov]

Similar symptoms