Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nicoleta Kiritescu"'
Publikováno v:
Romanian Journal of Pediatrics, Vol 65, Iss 1, Pp 60-62 (2016)
The Crouzon’s Syndrome is a rare genetic disorder, with an incidence between 1/25,000 to 1/100,000 newborn babies, transmitted autosomal dominant, characterized by facial dysmorphism and craniosynostosis, based on those characteristic can be diag
Externí odkaz:
https://doaj.org/article/f27abfc01ad4456b9103c3bb818ecf4d
Publikováno v:
Romanian Journal of Pediatrics, Vol 65, Iss 1, Pp 123-125 (2016)
Sindromul Crouzon este o boală genetică rară, cu o incidenţă între 1/25.000-1/100.000 de nou-născuţi, transmisă autozomal dominant, caracterizată prin craniosinostoză şi dismorfism facial caracteristic, putând fi diagnosticat precoce. Pr
Externí odkaz:
https://doaj.org/article/a00eb3dab920404fafe3a62cf4022913