Cargando…

Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?

The phenotypes of human imprinted neurogenetic disorders can be hypothesized as extreme alterations of typical human phenotypes. The imprinted neurogenetic disorder Prader-Willi syndrome (PWS) features covarying phenotypes that centrally involve altered social behaviors, attachment, mood, circadian...

Descripción completa

Detalles Bibliográficos
Autores principales:	Salminen, Iiro, Read, Silven, Crespi, Bernard
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731222/ https://www.ncbi.nlm.nih.gov/pubmed/36506301 http://dx.doi.org/10.3389/fgene.2022.1041943

Ejemplares similares

Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes
por: Salminen, Iiro Ilmari, et al.
Publicado: (2019)

Epigenetics in Prader-Willi Syndrome
por: Mendiola, Aron Judd P., et al.
Publicado: (2021)

Pharmacodynamic Gene Testing in Prader-Willi Syndrome
por: Forster, Janice, et al.
Publicado: (2020)

First Case Report of Prader–Willi-Like Syndrome in Colombia
por: Candelo, Estephania, et al.
Publicado: (2018)

A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics
por: Strom, Samuel P., et al.
Publicado: (2021)

Prader-Willi syndrome: reflections on seminal studies and future therapies
por: Chung, Michael S., et al.
Publicado: (2020)

Learning by observation and learning by doing in Prader-Willi syndrome
por: Foti, Francesca, et al.
Publicado: (2015)

Dynamic Changes in the Quantitative Electroencephalographic Spectrum During Attention Tasks in Patients With Prader–Willi Syndrome
por: Tsai, Li-Ping, et al.
Publicado: (2022)

The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study
por: Ahakoud, Mohamed, et al.
Publicado: (2023)

Irisin and the Metabolic Phenotype of Adults with Prader-Willi Syndrome
por: Hirsch, Harry J., et al.
Publicado: (2015)

Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015)

Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
por: Cheon, Chong Kun
Publicado: (2016)

Cerebellar Volumes Associate with Behavioral Phenotypes in Prader-Willi Syndrome
por: Yamada, Kenichi, et al.
Publicado: (2020)

Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome
por: Costa, Régis Afonso, et al.
Publicado: (2019)

PSIS With Phenotypic Features of Prader Willi and Fragile X Syndrome
por: Ali, Syeda Fatima, et al.
Publicado: (2021)

The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype
por: Holland, Anthony, et al.
Publicado: (2022)

AMBRA1, Autophagy, and the Extreme Male Brain Theory of Autism
por: Crespi, Bernard, et al.
Publicado: (2019)

Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families
por: Chen, XiaoFei, et al.
Publicado: (2023)

Do patients with Prader–Willi syndrome have favorable glucose metabolism?
por: Qian, Yanjie, et al.
Publicado: (2022)

Prader-Willi Syndrome: Clinical Aspects
por: Elena, Grechi, et al.
Publicado: (2012)

Hyperprolactinemia in Adults with Prader-Willi Syndrome
por: Sjöström, Anna, et al.
Publicado: (2021)

Approach to the Patient With Prader–Willi Syndrome
por: Höybye, Charlotte, et al.
Publicado: (2022)

Sleep Consequences of Prader-Willi Syndrome
por: Itani, Reem, et al.
Publicado: (2023)

Grey matter volume and cortical structure in Prader-Willi syndrome compared to typically developing young adults
por: Manning, Katherine E., et al.
Publicado: (2017)

Truncating mutations of MAGEL2cause Prader-Willi phenotypes and autism
por: Schaaf, Christian P., et al.
Publicado: (2013)

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome
por: Zhang, Lu, et al.
Publicado: (2022)

Causes of Death in Prader-Willi Syndrome: Prader-Willi Syndrome Association (USA) 40-Year Mortality Survey
por: Butler, Merlin G., et al.
Publicado: (2016)

Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
por: Heseding, Hannah M., et al.
Publicado: (2022)

PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW
por: Passone, Caroline Buff Gouveia, et al.
Publicado: (2018)

Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype
por: Whittington, Joyce, et al.
Publicado: (2022)

Prader-Willi syndrome: A primer for clinicians
por: Cataletto, Mary, et al.
Publicado: (2011)

Prader-Willi Syndrome and Growth Hormone Deficiency
por: Aycan, Zehra, et al.
Publicado: (2014)

Endocrine manifestations and management of Prader-Willi syndrome
por: Emerick, Jill E, et al.
Publicado: (2013)

Clinical and laboratory characteristics of Prader-Willi syndrome
por: Thao, Bui Phuong, et al.
Publicado: (2013)

Gall bladder agenesis in Prader Willi syndrome
por: Nair, Abilash, et al.
Publicado: (2015)

Adult Prader-Willi Syndrome: An Update on Management
por: Ho-Ming, Luk
Publicado: (2016)

Pituitary-Adrenal Axis in Prader Willi Syndrome
por: Edgar, Olivia S., et al.
Publicado: (2016)

Dietary Management for Adolescents with Prader–Willi Syndrome
por: Miller, Jennifer L, et al.
Publicado: (2020)

EEG Patterns in Patients with Prader–Willi Syndrome
por: Elia, Maurizio, et al.
Publicado: (2021)

Multidimensional Evaluation of Awareness in Prader-Willi Syndrome
por: Cobo, Jesús, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_indiv4iplcep9upu7np8h0rh0v