Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review

Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review

Kindler Syndrome (KS) is a rare, autosomal recessive genodermatosis caused by mutations in the FERMT1 gene, leading to skin fragility, blistering, photosensitivity, and progressive poikiloderma. We present a unique case of KS in a 6-year-old boy born to consanguineous parents, exhibiting uncommon de...

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Bibliographic Details
Main Authors: Muhammad Aamir, Fahad Faizullah, Malik W. Z. Khan, Touba Azeem, Muhammad Awais Khan
Format: Article
Language:English
Published: SAGE Publishing 2025-05-01
Series:Clinical Medicine Insights: Case Reports
Online Access:https://doi.org/10.1177/11795476251342637
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