An infant with lamellar ichthyosis presenting with meningitis

Autor:	Telila Mesfin, Mesfin Tsegaye, Kenbon Seyoum, Girma Geta, Neway Ejigu, Tesfaye Elala, Degefa Gomora, Biniyam Sahiledengle, Eshetu Mesfin Tadesse, Getu Kusa, Teketel Tilahun
Jazyk:	angličtina
Rok vydání:	2023
Předmět:	autosomal recessive infant lamellar ichthyosis skin hyperkeratinization Medicine Medicine (General) R5-920
Zdroj:	Clinical Case Reports, Vol 11, Iss 12, Pp n/a-n/a (2023)
Druh dokumentu:	article
ISSN:	2050-0904
DOI:	10.1002/ccr3.8329
Popis:	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.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/6044fc2c754a4e7fa6ffe2c00d6ef88d Zobrazit plný text záznamu View record in DOAJ Plný text ve formátu PDF Plný text ve formátu HTML
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