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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-[] These data define the clinical and molecular phenotype of neonatal-onset multisystem inflammatory disease as induced by interleukin-1β excess.[] 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[]

  • 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.[] 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.[] Escherichia coli: a growing problem in early onset neonatal sepsis. Aust N Z J Obstet Gynaecol 2004;44(6):558-61. 4.[]

  • Neonatal Infection

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

  • CINCA Syndrome

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

  • Muckle Wells Syndrome

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

  • Sepsis in Premature Infants

    neonatal sepsis (EONS) in preterm labor with premature rupture of membranes (PROM), allowing rational use of antibiotics.[] Management of neonates with suspected or proven early-onset bacterial sepsis.[] […] 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[]

  • Umbilical Sepsis

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

  • 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.[] Neonatal-onset CPSI deficiency is the most common form of the disease.[] Early liver transplantation for those with neonatal-onset CPS1D can correct metabolic abnormalities but does not reverse any neurological complications.[]

  • 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.[] , 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[] 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[]

  • 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.[] Clinical description Patients with MADD fall into 3 broad clinical phenotypes: 1) neonatal onset with congenital anomalies, 2) neonatal onset without anomalies, (together[] Characteristic phenotypes include the neonatal-onset (lethal) form with congenital abnormalities (type I), the neonatal-onset form with hypoketotic hypoglycemia without congenital[]

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