First documented case of Myhre syndrome in Romania: A case report

Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder, characterized by developmental delay, characteristic facial features, various bone and joint abnormalities, distinctive cardiovascular, ophthalmological and ear, nose and throat (ENT) manifestations, in association with...

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Detalles Bibliográficos
Autores principales: Cătană, Andreea, Simonescu-Colan, Ruxandra, Cuzmici-Barabaș, Zina, Militaru, Diana, Iordănescu, Irina, Militaru, Mariela Sanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972842/
https://www.ncbi.nlm.nih.gov/pubmed/35386616
http://dx.doi.org/10.3892/etm.2022.11252

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972842/
https://www.ncbi.nlm.nih.gov/pubmed/35386616
http://dx.doi.org/10.3892/etm.2022.11252

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