Congenital spondyloepiphyseal dysplasia
Introduction: congenital spondyloepiphyseal dysplasia, a type of bone dysplasia manifest from the infancy stage, is caused by mutations in the COL2A1 gene, located on chromosome 12, causing defects in type II collagen, a major component of cartilage. This type of collagen is also found in the vitreo...
Main Author: | Elayne Esther Santana |
---|---|
Format: | Article |
Language: | Spanish |
Published: |
ECIMED
2017-12-01
|
Series: | Revista de Ciencias Médicas de Pinar del Río |
Subjects: | |
Online Access: | http://www.revcmpinar.sld.cu/index.php/publicaciones/article/view/3296 |
Similar Items
-
Estudo das mutações no gene COL2A1 em uma coorte de pacientes com displasias esqueléticas do grupo colagenopatia tipo II segundo critérios clínico-radiológicos
by: Silveira, Karina da Costa, 1989-
Published: (2014) -
What is new in genetics and osteogenesis imperfecta classification?
by: Eugênia R. Valadares, et al.
Published: (2014-12-01) -
Neoplasia endocrina múltiple tipo 1
by: Mariela Larrandaburu, et al.
Published: (2008-09-01) -
Síndrome de Cohen. Presentación de un caso
by: Elayne Esther Santana Hernández, et al.
Published: (2014-04-01) -
Síndrome de Cohen. Presentación de un caso
by: Elayne Esther Santana Hernández, et al.
Published: (2014-04-01)