Cargando…
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life
OBJECTIVE: Early diagnosis is of proven benefit in Prader-Willi syndrome (PWS). We therefore examined key perinatal features to aid early recognition. METHODS: Data were collected from case records of subjects attending a multi-disciplinary clinic and from a retrospective birth questionnaire. RESULT...
Autores principales: | Çizmecioğlu, Filiz Mine, Jones, Jeremy Huw, Paterson, Wendy Forsyth, Kherra, Sakina, Kourime, Mariam, McGowan, Ruth, Shaikh, M. Guftar, Donaldson, Malcolm |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083474/ https://www.ncbi.nlm.nih.gov/pubmed/29553044 http://dx.doi.org/10.4274/jcrpe.0029 |
Ejemplares similares
-
Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre
por: Kherra, Sakina, et al.
Publicado: (2021) -
Pituitary-Adrenal Axis in Prader Willi Syndrome
por: Edgar, Olivia S., et al.
Publicado: (2016) -
Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015) -
The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype
por: Holland, Anthony, et al.
Publicado: (2022) -
Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
por: Cheon, Chong Kun
Publicado: (2016)