Cargando…
A novel pathogenic mutation of the CYP27B1 gene in a patient with vitamin D-dependent rickets type 1: a case report
BACKGROUND: Rickets can occur due to Vitamin D deficiency or defects in its metabolism. Three rare genetic types of rickets with different alterations of genes have been reported, including: Vitamin D dependent rickets type 1, Vitamin D dependent rickets type 2 or also known as Vitamin D resistant r...
Autores principales: | Babiker, Amir MI, Al Gadi, Iman, Al-Jurayyan, Nasir AM, Al Nemri, Abdulrahman MH, Al haboob, Ali Abdu N, Al Boukai, Ahmed Amer, Al Zahrani, Ali, Habib, Hanan Ahmed |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232664/ https://www.ncbi.nlm.nih.gov/pubmed/25371233 http://dx.doi.org/10.1186/1756-0500-7-783 |
Ejemplares similares
-
Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy
por: Mohamed, Sarar, et al.
Publicado: (2013) -
Congenital toxoplasmosis presenting as central diabetes insipidus in an infant: a case report
por: Mohamed, Sarar, et al.
Publicado: (2014) -
A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia: Molecular genetics report from Saudi Arabia
por: Mohamed, Sarar, et al.
Publicado: (2015) -
Miller Fischer and posterior reversible encephalopathy syndromes post COVID-19 infection
por: Al Haboob, Ali A.
Publicado: (2021) -
Imaging of disorder of sex development
por: AlJurayyan, Nasir
Publicado: (2013)