Urological Manifestations of Kindler Syndrome: A Case Report

Kindler syndrome is a rare autosomal recessive skin disorder. It results from mutation of the FERM domain containing kindlin-1 (FERMT1) that leads to loss of function of kindlin-1, which plays a role in keratinocyte adhesion, polarization, proliferation, and migration. It is characterized by skin bl...

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Detalles Bibliográficos
Autores principales: Ghorai, Rudra, Singh, Gurpremjit, Mittal, Ankur, Panwar, Vikas K, Talwar, Harkirat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167044/
https://www.ncbi.nlm.nih.gov/pubmed/35676982
http://dx.doi.org/10.7759/cureus.24758

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167044/
https://www.ncbi.nlm.nih.gov/pubmed/35676982
http://dx.doi.org/10.7759/cureus.24758

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