Cargando…

DNA methylation alterations in the genome of a toddler with cri‐du‐chat syndrome

This manuscript reports on genomewide epigenetic alterations in cri‐du‐chat syndrome related to a partial aneusomy of chromosome 5. A systematic analysis of these alterations will open up new possibilities for the prognostic evaluation of CDCS patients and the development of new therapeutic interven...

Descripción completa

Detalles Bibliográficos
Autores principales:	Naumova, Oxana Y., Rychkov, Sergey Y., Kuznetzova, Tatyana V., Odintsova, Veronika V., Kornilov, Sergey A., Grigorenko, Elena L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2017
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771924/ https://www.ncbi.nlm.nih.gov/pubmed/29375829 http://dx.doi.org/10.1002/ccr3.1274

Ejemplares similares

DNA Methylation Alterations in Blood Cells of Toddlers with Down Syndrome
por: Naumova, Oxana Yu., et al.
Publicado: (2021)

Effects of early social deprivation on epigenetic statuses and adaptive behavior of young children: A study based on a cohort of institutionalized infants and toddlers
por: Naumova, Oxana Yu., et al.
Publicado: (2019)

Cri du Chat syndrome
por: Cerruti Mainardi, Paola
Publicado: (2006)

Cri-du-chat syndrome
por: Nandhagopal, R., et al.
Publicado: (2014)

Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia
por: Kornilov, Sergey A., et al.
Publicado: (2019)

Educational Priorities for Children with Cri-Du-Chat Syndrome
por: Pituch, Keenan A., et al.
Publicado: (2009)

Determination of periodontopathogens in patients with Cri du chat syndrome
por: Ballesta-Mudarra, Sofía, et al.
Publicado: (2013)

Children and adults affected by Cri du Chat syndrome: Care's recommendations
por: Liverani, Maria Elena, et al.
Publicado: (2019)

Brain Stem Hypoplasia Associated with Cri-du-Chat Syndrome
por: Hong, Jin Ho, et al.
Publicado: (2013)

Anesthetic experience of a patient with cri du chat syndrome
por: Han, Insoo, et al.
Publicado: (2013)

Perioperative Care of a Child With Cri Du Chat Syndrome
por: Davis, Catherine, et al.
Publicado: (2020)

A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing
por: Gibitova, Ekaterina A., et al.
Publicado: (2022)

Discordance for Cri du Chat Syndrome in a dichorionic–diamniotic twin pregnancy
por: González-Comadran, Mireia, et al.
Publicado: (2015)

Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease
por: Holland, Petter, et al.
Publicado: (2022)

A clue in the diagnosis of Cri-du-chat syndrome: Pontine hypoplasia
por: Uzunhan, Tuğçe Aksu, et al.
Publicado: (2014)

Neoplasia in Cri du Chat Syndrome from Italian and German Databases
por: Guala, Andrea, et al.
Publicado: (2017)

Cri-Du-Chat Syndrome Associated With Meningomyelocele: A Case Report
por: Alabbad, Fatimah A, et al.
Publicado: (2023)

Congenital vertical talus in Cri du Chat Syndrome: a case report
por: Khader, Amani, et al.
Publicado: (2013)

Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome
por: Peng, Ying, et al.
Publicado: (2020)

Cri du chat syndrome and autism spectrum disorder: a case report
por: Raissouni, M., et al.
Publicado: (2023)

Laboratorio clínico, Síndrome de Cri Du Chat y su historia natural
por: Pulido Espinosa, Celina de Jesús
Publicado: (1993)

Le syndrome de Cri du Chat : A propos d’une observation
por: Ouldim, Karim, et al.
Publicado: (2012)

Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients
por: Espirito Santo, Layla Damasceno, et al.
Publicado: (2016)

Neonatal Cri du chat syndrome with atypical facial appearance: A case report
por: Bai, Meng-Meng, et al.
Publicado: (2022)

Social Economic Costs, Health-Related Quality of Life and Disability in Patients with Cri Du Chat Syndrome
por: Kodra, Yllka, et al.
Publicado: (2020)

Male pseudohermaphroditism: A case study of 46,XY disorder of sexual development using whole‐exome sequencing
por: Naumova, Oxana Yu., et al.
Publicado: (2020)

Language Outcomes in Adults with a History of Institutionalization: Behavioral and Neurophysiological Characterization
por: Kornilov, Sergey A., et al.
Publicado: (2019)

Difficult airway management and suspected malignant hyperthermia in a Child with Cri Du Chat Syndrome
por: Amata, Andrew O.
Publicado: (2019)

Tubo-ovarian abscess in a patient with cri du chat syndrome: A case report
por: Fujimori, Mimori, et al.
Publicado: (2022)

Psychomotor Development in Cri du Chat Syndrome: Comparison in Two Italian Cohorts with Different Rehabilitation Methods
por: Guala, Andrea, et al.
Publicado: (2016)

Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature
por: Su, Jiasun, et al.
Publicado: (2019)

Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review
por: Traisrisilp, Kuntharee, et al.
Publicado: (2022)

Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome
por: Sheth, Frenny, et al.
Publicado: (2012)

Effects of Oral Stimulation Intervention in Newborn Babies with Cri du Chat Syndrome: Single-Subject Research Design
por: Kim, Mi Kyung, et al.
Publicado: (2018)

Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report
por: Vado, Yerai, et al.
Publicado: (2018)

Difficult intubation caused by an immature upper airway in a patient with cri-du-chat syndrome: a case report
por: So, Eunsun, et al.
Publicado: (2020)

Integrated analysis of the critical region 5p15.3–p15.2 associated with cri-du-chat syndrome
por: Corrêa, Thiago, et al.
Publicado: (2019)

The psychometric properties of the Quantitative-Checklist for Autism in Toddlers (Q-CHAT) as a measure of autistic traits in a community sample of Singaporean infants and toddlers
por: Magiati, I., et al.
Publicado: (2015)

Age-related Behavioural Change in Cornelia de Lange and Cri du Chat Syndromes: A Seven Year Follow-up Study
por: Cochran, Lisa, et al.
Publicado: (2019)

Parent-Endorsed Sex Differences in Toddlers with and Without ASD: Utilizing the M-CHAT
por: Øien, Roald A., et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_hl9tov90f52n4iq1cudnlt0qme