Early-Age Manifestation of Singleton Merten Syndrome With Systemic Lupus Erythematosus Features: A Case Report

Singleton Merten syndrome (SMS) is one of the rarest multisystem genetic disorders that had been recognized in only a few cases. Patients who have this syndrome often present with calcification of the aorta and heart valves, dental dysplasia, joint calcification, distinct facial features, and growth...

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Detalles Bibliográficos
Autores principales: Alzahrani, Yazeed M, Alamoudi, Ahmad A, Nahar, Nojoud K, Albar, Rawia F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217668/
https://www.ncbi.nlm.nih.gov/pubmed/35755559
http://dx.doi.org/10.7759/cureus.25244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217668/
https://www.ncbi.nlm.nih.gov/pubmed/35755559
http://dx.doi.org/10.7759/cureus.25244

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