An infant with lamellar ichthyosis presenting with meningitis.
autosomal recessive
infant
lamellar ichthyosis
skin hyperkeratinization
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
received:
04
08
2023
revised:
28
10
2023
accepted:
29
11
2023
medline:
13
12
2023
pubmed:
13
12
2023
entrez:
13
12
2023
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 38089483
doi: 10.1002/ccr3.8329
pii: CCR38329
pmc: PMC10710960
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e8329Informations de copyright
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
The authors declare that they have no conflicts of interest.