Kindler Syndrome Latest Advances

Co-occurrence of two monogenic diseases within a single family.

Journal: European journal of dermatology : EJD

Published: November 24, 2025

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

Kindler Syndrome: A Case Report From a Developing Country.

Journal: Clinical case reports

Published: March 03, 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

Kindler Syndrome in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report.

Journal: Case reports in dermatological medicine

Published: September 22, 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

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Co-occurrence of two monogenic diseases within a single family.

Co-occurrence of two monogenic diseases within a single family.

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.

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.

Kindler Syndrome: A Case Report From a Developing Country.

Kindler Syndrome: A Case Report From a Developing Country.

Cytomegalovirus Colitis in 2 Patients With Kindler Syndrome.

Cytomegalovirus Colitis in 2 Patients With Kindler Syndrome.

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 in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report.

Kindler Syndrome in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report.

Photobiomodulation Therapy in Improving Quality of Life in Kindler Syndrome: A Case Study.

Photobiomodulation Therapy in Improving Quality of Life in Kindler Syndrome: A Case Study.

Orofacial Manifestations of Kindler Epidermolysis Bullosa-Reply.

Orofacial Manifestations of Kindler Epidermolysis Bullosa-Reply.

Orofacial Manifestations of Kindler Epidermolysis Bullosa.

Orofacial Manifestations of Kindler Epidermolysis Bullosa.

Unusual oral manifestation of Kindler syndrome: a case report and review of literature.

Unusual oral manifestation of Kindler syndrome: a case report and review of literature.

Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients.

Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients.

Dermoscopic Correlation of an Eccentric Case of Kindler Syndrome.

Dermoscopic Correlation of an Eccentric Case of Kindler Syndrome.