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Last Updated: 10/31/2025
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Found 180 publications
A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions.
Journal: International journal of molecular sciences
Published: April 02, 2025
Cytomegalovirus Colitis in 2 Patients With Kindler Syndrome.
Journal: The Pediatric infectious disease journal
Published: February 17, 2025
Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review.
Journal: Clinical medicine insights. Case reports
Published: December 24, 2024
Photobiomodulation Therapy in Improving Quality of Life in Kindler Syndrome: A Case Study.
Journal: Journal of lasers in medical sciences
Published: September 16, 2024
Orofacial Manifestations of Kindler Epidermolysis Bullosa-Reply.
Journal: JAMA dermatology
Published: September 04, 2024
Orofacial Manifestations of Kindler Epidermolysis Bullosa.
Journal: JAMA dermatology
Published: September 04, 2024
Unusual oral manifestation of Kindler syndrome: a case report and review of literature.
Journal: Frontiers in oral health
Published: May 10, 2024
Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients.
Journal: Frontiers in pediatrics
Published: April 29, 2024
Dermoscopic Correlation of an Eccentric Case of Kindler Syndrome.
Journal: Cureus
Published: April 16, 2024
Battling a rarity: A case of kindler syndrome from a developing country.
Journal: SAGE open medical case reports
Published: November 18, 2023
Kindler syndrome with a novel mutation and gynaecological complication.
Journal: Clinical and experimental dermatology
Published: August 17, 2023
Last Updated: 10/31/2025