Cargando…
Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force
BACKGROUND: Ring chromosome 14 syndrome is a rare chromosomal disorder characterized by early onset refractory epilepsy, intellectual disability, autism spectrum disorder and a number of diverse health issues. RESULTS: The aim of this work is to provide recommendations for the diagnosis and manageme...
Autores principales: | Rinaldi, Berardo, Vaisfeld, Alessandro, Amarri, Sergio, Baldo, Chiara, Gobbi, Giuseppe, Magini, Pamela, Melli, Erto, Neri, Giovanni, Novara, Francesca, Pippucci, Tommaso, Rizzi, Romana, Soresina, Annarosa, Zampini, Laura, Zuffardi, Orsetta, Crimi, Marco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387247/ https://www.ncbi.nlm.nih.gov/pubmed/28399932 http://dx.doi.org/10.1186/s13023-017-0606-4 |
Ejemplares similares
-
A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy
por: Caretto, Amelia, et al.
Publicado: (2014) -
SMARCA4 inactivating mutations cause concomitant Coffin–Siris syndrome, microphthalmia and small‐cell carcinoma of the ovary hypercalcaemic type
por: Errichiello, Edoardo, et al.
Publicado: (2017) -
MECP2 duplication phenotype in symptomatic females: report of three further cases
por: Novara, Francesca, et al.
Publicado: (2014) -
Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature
por: Errichiello, Edoardo, et al.
Publicado: (2016) -
Ad Hoc Discussion Session
por: Reich, Κ Η
Publicado: (1974)