Cargando…
Wolcott-Rallison syndrome: a case series of three patients
INTRODUCTION: Neonatal diabetes is a rare disease with incidence estimated at 1 in 300,000 to 1 in 400,000 live births. Walcott-Rallison syndrome has been identified as the most common cause of permanent neonatal diabetes in consanguineous families caused by mutations in eukaryotic translation initi...
Autores principales: | Memon, Fozia, Arif, Muzna, Kirmani, Salman, Humayun, Khadija N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214929/ https://www.ncbi.nlm.nih.gov/pubmed/36106422 http://dx.doi.org/10.5114/pedm.2022.118325 |
Ejemplares similares
-
Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 gene
por: Gupta, Atul, et al.
Publicado: (2021) -
Wolcott-Rallison syndrome
por: Julier, Cécile, et al.
Publicado: (2010) -
Wolcott-Rallison syndrome in a Bedouin boy
por: Marafie, Makia J., et al.
Publicado: (2004) -
Silver-Russell syndrome and Turner syndrome in a girl with short stature treated with growth hormone – case report
por: Wikiera, Beata, et al.
Publicado: (2022) -
Endocrine disorders in a patient with a suspicion of a mitochondrial disease, MELAS syndrome – a case report and literature review
por: Baszyńska-Wilk, Marta, et al.
Publicado: (2021)