Cargando…
Gorlin-Goltz syndrome
Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. The authors present a case of an 11-year-old girl with typical features of Gorlin-Goltz syndrome with special respect to medical and dental problems which include multiple bo...
Autores principales: | Kohli, Munish, Kohli, Monica, Sharma, Naresh, Siddiqui, Saif Rauf, Tulsi, S.P.S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304191/ https://www.ncbi.nlm.nih.gov/pubmed/22442551 http://dx.doi.org/10.4103/0975-5950.69171 |
Ejemplares similares
-
Gorlin-Goltz syndrome
por: Jawa, Deepti Singh, et al.
Publicado: (2009) -
Gorlin-Goltz syndrome
por: Joshi, Priya Shirish, et al.
Publicado: (2012) -
Gorlin-Goltz Syndrome
por: Pandeshwar, Padma, et al.
Publicado: (2012) -
Gorlin-Goltz Syndrome
por: Mehta, DN, et al.
Publicado: (2014) -
Gorlin-Goltz syndrome with situs oppositus
por: Guruprasad, Yadavalli, et al.
Publicado: (2010)