Ichthyosis Prematurity Syndrome: A Rare Form but Easily Recognizable Ichthyosis

Ichthyosis Prematurity Syndrome: A Rare Form but Easily Recognizable Ichthyosis

Ichthyosis prematurity syndrome is a rare autosomal recessive genodermatosis that is associated with mutations in the SLC27A4 gene. Its onset occurs in early childhood and presents with the clinical triad of premature birth, thick caseous desquamating epidermis, and neonatal asphyxia. Here, we descr...

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Bibliographic Details
Main Authors: Sultan Al-Khenaizan, Asma AlSwailem, Mohammed Ali AlBalwi
Format: Article
Language:English
Published: Karger Publishers 2021-09-01
Series:Case Reports in Dermatology
Subjects:
ichthyosis prematurity syndrome
solute carrier family 27 member 4
verruciform hyperkeratotic plaques
cobblestone appearance
premature birth
neonatal asphyxia
Online Access:https://www.karger.com/Article/FullText/519035

Internet

https://www.karger.com/Article/FullText/519035

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