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An infant with lamellar ichthyosis presenting with meningitis.
Mesfin, Telila; Tsegaye, Mesfin; Seyoum, Kenbon; Geta, Girma; Ejigu, Neway; Elala, Tesfaye; Gomora, Degefa; Sahiledengle, Biniyam; Tadesse, Eshetu Mesfin; Kusa, Getu; Tilahun, Teketel.
Afiliação
  • Mesfin T; School of Medicine Goba General Hospital Goba Ethiopia.
  • Tsegaye M; School of Medicine Goba General Hospital Goba Ethiopia.
  • Seyoum K; Department of Midwifery Goba General Hospital Goba Ethiopia.
  • Geta G; Department of Midwifery Goba General Hospital Goba Ethiopia.
  • Ejigu N; Department of Midwifery Goba General Hospital Goba Ethiopia.
  • Elala T; Department of Pediatrics Goba General Hospital Goba Ethiopia.
  • Gomora D; Department of Midwifery Goba General Hospital Goba Ethiopia.
  • Sahiledengle B; Department of Public Health Goba General Hospital Goba Ethiopia.
  • Tadesse EM; Department of Public Health ICAP Addis Ababa Ethiopia.
  • Kusa G; School of Medicine Goba General Hospital Goba Ethiopia.
  • Tilahun T; Department of Public Health Menilik II Comprehensive Specialized Hospital Addis Ababa Ethiopia.
Clin Case Rep ; 11(12): e8329, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38089483
ABSTRACT
Lamellar ichthyosis is a rare congenital disorder characterized by widespread epidermal hyperkeratinization. It is a rare clinical disorder throughout the entire planet, and newborns with this disease frequently have collodion membranes (adhering, supple, parchment-like membrane). We present a 45-day-old infant who came to our facility complaining of a high-grade persistent fever, high-pitched crying, decreased feeding, odd body movements, rapid breathing, and grunting that lasted for 2 days. He was diagnosed with lamellar ichthyosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article