Cargando…
Computer-aided facial analysis as a tool to identify patients with Silver–Russell syndrome and Prader–Willi syndrome
Genetic syndromes often show facial features that provide clues for the diagnosis. However, memorizing these features is a challenging task for clinicians. In the last years, the app Face2Gene proved to be a helpful support for the diagnosis of genetic diseases by analyzing features detected in one...
Autores principales: | Ciancia, Silvia, Goedegebuure, Wesley J., Grootjen, Lionne N., Hokken-Koelega, Anita C. S., Kerkhof, Gerthe F., van der Kaay, Daniëlle C. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257592/ https://www.ncbi.nlm.nih.gov/pubmed/36947243 http://dx.doi.org/10.1007/s00431-023-04937-x |
Ejemplares similares
-
Atypical 15q11.2-q13 Deletions and the Prader-Willi Phenotype
por: Grootjen, Lionne N., et al.
Publicado: (2022) -
Prenatal and Neonatal Characteristics of Children with Prader-Willi Syndrome
por: Grootjen, Lionne N., et al.
Publicado: (2022) -
Acute stress response of the HPA-axis in children with Prader-Willi syndrome: new insights and consequences for clinical practice
por: Grootjen, Lionne N., et al.
Publicado: (2023) -
Evidence for Accelerated Biological Aging in Young Adults with Prader–Willi Syndrome
por: Donze, Stephany H, et al.
Publicado: (2019) -
Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
por: Damen, Layla, et al.
Publicado: (2020)