Cargando…
Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
Urea cycle disorders (UCDs) are an unusual genetic condition that may lead to hyperammonemia in catabolic situations such as surgery, infections or chemotherapy administration. Without specific treatment, it causes life-threatening encephalopathy. We present the case of a young woman, heterozygous c...
Autores principales: | Palka-Kotlowska, Magda, Cabezón-Gutiérrez, Luis, Custodio-Cabello, Sara, Quijada-Fraile, PIlar, Chumillas-Calzada, Silvia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317123/ https://www.ncbi.nlm.nih.gov/pubmed/32601573 http://dx.doi.org/10.7759/cureus.8301 |
Ejemplares similares
-
Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency
por: Eskander, Peter N, et al.
Publicado: (2021) -
Antepartum Ornithine Transcarbamylase Deficiency
por: Nakajima, Hitoshi, et al.
Publicado: (2014) -
Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency
por: Li, Sitao, et al.
Publicado: (2018) -
Ornithine transcarbamylase deficiency: A diagnostic odyssey
por: Knerr, Ina, et al.
Publicado: (2022) -
Three-Country Snapshot of Ornithine Transcarbamylase Deficiency
por: Seker Yilmaz, Berna, et al.
Publicado: (2022)