Cargando…
An interesting case of familial chylomicronemia syndrome in a cleft palate child
Familial chylomicronemia syndrome is a very rare condition with an incidence of one in one million. We report such a condition detected incidentally in a cleft child.
Autores principales: | Adenwalla, H. S., Narayanan, P. V., Rajshree, C. J., Santhakumar, Rati |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739552/ https://www.ncbi.nlm.nih.gov/pubmed/19753206 http://dx.doi.org/10.4103/0970-0358.41116 |
Ejemplares similares
-
A case report of acampomelic campomelic dysplasia and operative difficulties in cleft palate reconstruction
por: Pasupathy, M., et al.
Publicado: (2016) -
Two Case Reports of Familial Chylomicronemia Syndrome
por: Chen, Yan-Hui, et al.
Publicado: (2012) -
Familial chylomicronemia syndrome: a case report
por: Susheela, Ammu Thampi, et al.
Publicado: (2021) -
Vomerine hamartoma in a cleft palate child
por: Bang, Rameshwar L., et al.
Publicado: (2010) -
Cleft palate in Williams syndrome
por: Domenico, Scopelliti, et al.
Publicado: (2013)