Kindler syndrome: a rare case report from Syria

Kindler syndrome is a rare autosomal recessive inherited disease. The authors report a case with unique presentation that has never reported before in the medical Literatur” lanugo hair”. This is a case of a 13-year-old Syrian child, who presented with difuse fine face hair, and serious urinary comp...

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Detalles Bibliográficos
Autores principales: Edrees, Souma, Jarkas, Natalie, Hraib, Munawar, Al-Yousef, Khaled, Baddour, Roula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205305/
https://www.ncbi.nlm.nih.gov/pubmed/37229095
http://dx.doi.org/10.1097/MS9.0000000000000503

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205305/
https://www.ncbi.nlm.nih.gov/pubmed/37229095
http://dx.doi.org/10.1097/MS9.0000000000000503

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