Cargando…
Systemic Lupus Erythematosus and Hereditary Coproporphyria: Two Different Entities Diagnosed by WES in the Same Patient
BACKGROUND: Hereditary coproporphyria (HCP) is a rare autosomal dominant disorder caused by a partial deficiency of coproporphyrinogen III oxidase (CPOX), and systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic predisposition. SLC7A7 (solute carrier family 7 member 7) m...
Autores principales: | Liu, Anlei, Zhou, Lingli, Zhu, Huadong, Li, Yi, Yang, Jing |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167117/ https://www.ncbi.nlm.nih.gov/pubmed/35669728 http://dx.doi.org/10.1155/2022/9096999 |
Ejemplares similares
-
Hereditary coproporphyria.
por: Paterson, A., et al.
Publicado: (1994) -
Neuropathic pain in hereditary coproporphyria
por: Chen, Guan-Liang, et al.
Publicado: (2013) -
Delirium with delayed diagnosis of hereditary coproporphyria
por: Eroglu, Seyma, et al.
Publicado: (2022) -
P01-026 – A case of FMF and hereditary coproporphyria
por: Ganesha, A, et al.
Publicado: (2013) -
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
por: Conway, Ashlee J., et al.
Publicado: (2017)