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Subdural hemorrhage, macrocephaly, rash, and developmental delay in an infant: A pathogenic variant in NLRP3 causes CINCA/NOMID.
Koti, Ajay S; Lanis, Aviya; Finlayson, Samuel; Canny, Susan; Feldman, Elana A; Miller, Danny E; Rosenwasser, Natalie; Scott, Abbey A; Wong, Stephen C; Feldman, Kenneth W.
Afiliação
  • Koti AS; Safe Child and Adolescent Network, Department of Pediatrics, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Lanis A; Division of Rheumatology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Finlayson S; Division of Genetic Medicine, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Canny S; Division of Rheumatology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Feldman EA; Safe Child and Adolescent Network, Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
  • Miller DE; Division of Genetic Medicine, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Rosenwasser N; Division of Rheumatology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Scott AA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Wong SC; Division of Rheumatology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Feldman KW; Safe Child and Adolescent Network, Department of Pediatrics, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
Am J Med Genet A ; 191(12): 2825-2830, 2023 12.
Article em En | MEDLINE | ID: mdl-37548074
Subdural hemorrhages (SDHs) in children are most often observed in abusive head trauma (AHT), a distinct form of traumatic brain injury, but they may occur in other conditions as well, typically with clear signs and symptoms of an alternative diagnosis. We present a case of an infant whose SDH initially raised the question of AHT, but multidisciplinary evaluation identified multiple abnormalities, including rash, macrocephaly, growth failure, and elevated inflammatory markers, which were all atypical for trauma. These, along with significant cerebral atrophy, ventriculomegaly, and an absence of other injuries, raised concerns for a genetic disorder, prompting genetic consultation. Clinical trio exome sequencing identified a de novo likely pathogenic variant in NLRP3, which is associated with chronic infantile neurological, cutaneous, and articular (CINCA) syndrome, also known as neonatal-onset multisystem inflammatory disease (NOMID). He was successfully treated with interleukin-1 blockade, highlighting the importance of prompt treatment in CINCA/NOMID patients. This case also illustrates how atraumatic cases of SDH can be readily distinguished from AHT with multidisciplinary collaboration and careful consideration of the clinical history and exam findings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Maus-Tratos Infantis / Exantema / Síndromes Periódicas Associadas à Criopirina / Megalencefalia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Maus-Tratos Infantis / Exantema / Síndromes Periódicas Associadas à Criopirina / Megalencefalia Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article