Cargando…
The case of a patient with MIRAGE syndrome with familial dysautonomia-like symptoms
We describe a case of posthumously diagnosed MIRAGE syndrome (Myelodysplasia, Infection, Restriction of growth, Adrenal hypoplasia, Genital problems, and Enteropathy) in a girl with a new pathogenic SAMD9 variant (p.F437S), who was initially considered to have familial dysautonomia (FD)-like disease...
Autores principales: | Kawashima-Sonoyama, Yuki, Okuno, Keisuke, Dohmoto, Tomotsune, Tanase-Nakao, Kanako, Narumi, Satoshi, Namba, Noriyuki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275606/ https://www.ncbi.nlm.nih.gov/pubmed/34253717 http://dx.doi.org/10.1038/s41439-021-00158-6 |
Ejemplares similares
-
MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene
por: Onuma, Shinsuke, et al.
Publicado: (2020) -
Acquired uniparental disomy of chromosome 7 in a patient with MIRAGE syndrome
that veiled a pathogenic SAMD9 variant
por: Tanase-Nakao, Kanako, et al.
Publicado: (2021) -
A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report
por: Ishiwa, Sho, et al.
Publicado: (2020) -
MIRAGE syndrome with recurrent pneumonia probably associated with
gastroesophageal reflux and achalasia: A case report
por: Yoshizaki, Kanako, et al.
Publicado: (2019) -
Familial Dysautonomia: Mechanisms and Models
por: Dietrich, Paula, et al.
Publicado: (2016)