Cargando…
Cornelia De-Lange Syndrome: A Case Report
Cornelia de-Lange syndrome is a congenital anomaly syndrome characterized by distinctive facial dysmorphism, primordial short stature, hirsutism, and upper limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly. Craniofacial features include synophrys, arched eyebrows...
Autores principales: | Mehta, Diana Noshir, Bhatia, Rupinder |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086580/ https://www.ncbi.nlm.nih.gov/pubmed/25206204 http://dx.doi.org/10.5005/jp-journals-10005-1201 |
Ejemplares similares
-
Cornelia de lange syndrome
por: Tayebi, Naeimeh
Publicado: (2008) -
Case Report: Atypical Cornelia de Lange Syndrome
por: Leanza, Vito, et al.
Publicado: (2015) -
Dental Findings in Cornelia De Lange Syndrome
por: Toker, Aslihan Soyal, et al.
Publicado: (2009) -
Cornelia De Lange Syndrome and Cochlear Implantation
por: Psillas, George, et al.
Publicado: (2018) -
A newborn with Cornelia de Lange syndrome: a case report
por: Uzun, Hakan, et al.
Publicado: (2008)