Cargando…
Goldenhar Syndrome: A Case Report
BACKGROUND: Goldenhar syndrome is a multiple congenital disorder with classic characteristics regarding the face, eyes, ears. The incidence of this case is between 1:3.500 to 1:5.600. Early detection and good management can have good outcomes. A newborn with this condition can have a normal life and...
Autores principales: | Kurniawan, Ruby, Suarca, I Kadek, Suryawan, I Wayan Bikin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Republic of Macedonia
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514341/ https://www.ncbi.nlm.nih.gov/pubmed/31110581 http://dx.doi.org/10.3889/oamjms.2019.281 |
Ejemplares similares
-
Osteoporosis resulting from acute lymphoblastic leukemia in a 7-year-old boy: a case report
por: Salim, Hendra, et al.
Publicado: (2014) -
Goldenhar Syndrome: A rare case report
por: Bhuyan, Ruchi, et al.
Publicado: (2016) -
Goldenhar Syndrome: A Case Report with Review
por: Goswami, Mridula, et al.
Publicado: (2016) -
The Association between Obesity and Severity of Dengue Hemorrhagic Fever in Children at Wangaya General Hospital
por: Kurnia, Bella, et al.
Publicado: (2019) -
Iodine status as indited by neonatal thyroid stimulating hormone screening in Mitre Keluarga Hospital in Surabaya at 2005-2010
por: Untario, Connie, et al.
Publicado: (2013)