Clinical and genetic features of four patients with Pearson syndrome: An observational study

Pearson syndrome (PS) is a multisystem mitochondrial cytopathy arising from deletions in mitochondrial DNA. Pearson syndrome is a sporadic disease that affects the hematopoietic system, pancreas, eyes, liver, and heart and the prognosis is poor. Causes of morbidity include metabolic crisis, bone mar...

Descripción completa

Detalles Bibliográficos
Autores principales: Son, Ji Soo, Seo, Go Hun, Kim, Yoon-Myung, Kim, Gu-Hwan, Jin, Hee Kyung, Bae, Jae-sung, Im, Ho Joon, Yoo, Han-Wook, Lee, Beom Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812667/
https://www.ncbi.nlm.nih.gov/pubmed/35119049
http://dx.doi.org/10.1097/MD.0000000000028793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812667/
https://www.ncbi.nlm.nih.gov/pubmed/35119049
http://dx.doi.org/10.1097/MD.0000000000028793

Ejemplares similares