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3,078 Possible Causes for Neonate-Onset

  • Cryopyrin-Associated Periodic Syndrome

    Onset Multisystem Inflammatory Disease (NOMID) or Neonatal Onset Multisystem Inflammatory Disease (NOMID), children, systemic autoinflammatory disease, CIAS-1 gene, NALP-[clinicaltrials.gov] These data define the clinical and molecular phenotype of neonatal-onset multisystem inflammatory disease as induced by interleukin-1β excess.[doi.org] Clinical and epidemiological research A 24-month open-label study of canakinumab in neonatal-onset multisystem inflammatory disease Cailin H Sibley 1, Andrea Chioato 2, Sandra[doi.org]

  • Neonatal Sepsis

    Wortham JM, Hansen NI, Schrag SJ, et al; Eunice Kennedy Shriver NICHD Neonatal Research Network. Chorioamnionitis and culture-confirmed, early-onset neonatal infections.[jamanetwork.com] Mishra UK, Jacobs SE, Doyle LW, Garland SM (2006) Newer approaches to the diagnosis of early onset neonatal sepsis. Arch Dis Child Fetal Neonatal Ed 91: F208-212.[omicsonline.org] Escherichia coli: a growing problem in early onset neonatal sepsis. Aust N Z J Obstet Gynaecol 2004;44(6):558-61. 4.[imj.ie]

  • Neonatal Infection

    neonatal infection and Table 2 below to identify clinical indicators of early-onset neonatal infection.[web.archive.org] KEYWORDS: C-reactive protein; antibiotic therapy; early-onset neonatal sepsis; procalcitonin; white blood cell count[ncbi.nlm.nih.gov] Our results indicate that sRAGE could be a good potential biomarker of late-onset neonatal infection and sepsis (Tab. 2, Ref. 14).[ncbi.nlm.nih.gov]

  • CINCA Syndrome

    Multisystem Inflammatory Disease; IOMID; NOMID; Multisystem inflammatory disease, neonatal-onset; Prieur Griscelli syndrome See More Categories: Neonatal onset multisystem[rarediseases.info.nih.gov] Neonatal-onset multisystem inflammatory disease is a rare genetic periodic fever syndrome which causes uncontrolled inflammation in multiple parts of the body starting in[en.wikipedia.org] Clinical Research Resources ClinicalTrials.gov lists trials that are related to Neonatal Onset Multisystem Inflammatory disease.[rarediseases.info.nih.gov]

  • Muckle Wells Syndrome

    Neonatal-onset multisystem inflammatory disease (NOMID)/chronic infantile neurologic, cutaneous, and articular syndrome is an autoinflammatory disease characterized by urticarial[ncbi.nlm.nih.gov] Salford Royal NHS Foundation Trust, Manchester, UK. vishalmadan@doctors.org.uk Abstract We describe a patient with overlapping clinical features of Muckle-Wells syndrome and neonatal-onset[ncbi.nlm.nih.gov] onset multisystem inflammatory disease, also called chronic, infantile, neurological, cutaneous, and articular syndrome, are three hereditary autoinflammatory syndromes caused[doi.org]

  • Sepsis in Premature Infants

    neonatal sepsis (EONS) in preterm labor with premature rupture of membranes (PROM), allowing rational use of antibiotics.[onlinelibrary.wiley.com] Management of neonates with suspected or proven early-onset bacterial sepsis.[ncbi.nlm.nih.gov] […] and mortality, and is an ongoing major global public health challenge. 1 According to the onset of age, neonatal sepsis is divided into early-onset sepsis (EOS) and late-onset[fn.bmj.com]

  • Umbilical Sepsis

    SETTING Evaluation of umbilical cord IL-6 and funisitis as predictors of early-onset neonatal sepsis in PPROM.[semanticscholar.org] […] early onset sepsis.[karger.com] Biol Neonate 1996;70:206–212.[karger.com]

  • Carbamoyl Phosphate Synthetase Deficiency

    . [4] Severe hyperammonemia and severe clinical manifestations are common in neonatal-onset CPS1D. [1] Neonatal-onset patients are often born normally.[journals.lww.com] Neonatal-onset CPSI deficiency is the most common form of the disease.[symptoma.com] Early liver transplantation for those with neonatal-onset CPS1D can correct metabolic abnormalities but does not reverse any neurological complications.[orpha.net]

  • Severe Neonatal-Onset Encephalopathy with Microcephaly

    Severe neonatal-onset encephalopathy with microcephaly is an x-linked recessive disorder caused by mutations of the MECP2 gene. b' ' Systematic References: 1.[moldiag.com] , susceptibility to, X-linked 3 Angelman syndrome Severe neonatal-onset encephalopathy with microcephaly Mental retardation, X-linked, syndromic 13 Reversed 1 HGVS NC_000023.10[snpedia.com] ClinVar Risk rs28934906(T;T) Alt rs28934906(T;T) Reference Rs28934906(C;C) Significance Other Disease Rett syndrome Encephalopathy not provided Autism Angelman syndrome Severe neonatal-onset[snpedia.com]

  • Glutaric Aciduria Type 2

    Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.[uniprot.org] Clinical description Patients with MADD fall into 3 broad clinical phenotypes: 1) neonatal onset with congenital anomalies, 2) neonatal onset without anomalies, (together[orpha.net] Characteristic phenotypes include the neonatal-onset (lethal) form with congenital abnormalities (type I), the neonatal-onset form with hypoketotic hypoglycemia without congenital[medlink.com]

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