Cargando…

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature

The current study presents the cases of two unrelated patients with similar clinical features, including craniofacial anomalies, developmental delay/intellectual disability and cardiac malformations, that are consistent with chromosome 10q26 deletion syndrome. High-resolution single-nucleotide polym...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lin, Shaobin, Zhou, Yi, Fang, Qun, Wu, Jianzhu, Zhang, Zhiqiang, Ji, Yuanjun, Luo, Yanmin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2016
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355737/ https://www.ncbi.nlm.nih.gov/pubmed/27779662 http://dx.doi.org/10.3892/mmr.2016.5864

Ejemplares similares

Deletion mapping on chromosome 10q25-q26 in human endometrial cancer.
por: Nagase, S., et al.
Publicado: (1996)

An Interstitial Deletion at 10q26.2q26.3
por: Iourov, Ivan Y., et al.
Publicado: (2014)

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature
por: Popescu, Roxana, et al.
Publicado: (2021)

Chromosome 11q13 deletion syndrome
por: Kim, Yu-Seon, et al.
Publicado: (2016)

Deletion polymorphism at chromosome 3q26.1 and oral squamous cell carcinoma
por: KAWACHI, HOMARE, et al.
Publicado: (2012)

Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature review
por: Li, Qinghong, et al.
Publicado: (2021)

Case Report: Two New Cases of Chromosome 12q14 Deletions and Review of the Literature
por: Deng, Ruizhi, et al.
Publicado: (2021)

Identification of a common deletion region in 10q26 associated with human gliomas
por: Alves, Margarida, et al.
Publicado: (2010)

Isolated Chromosome 6q27 Terminal Deletion Syndrome
por: Bhatta, Sabita, et al.
Publicado: (2020)

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
por: Vona, Barbara, et al.
Publicado: (2014)

Mild Phenotype in a Patient with a De Novo 6.3 Mb Distal Deletion at 10q26.2q26.3
por: Tanteles, George A., et al.
Publicado: (2015)

Clinical variability of chromosome 22q11.2 deletion syndrome
por: Boyarchuk, Oksana, et al.
Publicado: (2017)

Dopaminergic neurons in chromosome 22q11.2 deletion syndrome
por: Inoue, Haruhisa
Publicado: (2021)

A case of myelodysplastic syndrome with t(10;18)(q26;q21)
por: Ohba, Yusuke, et al.
Publicado: (2019)

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families
por: HUANG, LINHUAN, et al.
Publicado: (2015)

The Second Case of Non-Mosaic Trisomy of Chromosome 26 with Homologous Fusion 26q;26q in the Horse
por: Ghosh, Sharmila, et al.
Publicado: (2022)

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family
por: Lin, Shaobin, et al.
Publicado: (2021)

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
por: Chang, Yu-Tzu, et al.
Publicado: (2014)

Chromosome 13q deletion syndrome involving 13q31-qter: A case report
por: Wang, Yue-Ping, et al.
Publicado: (2017)

Two Cases of Chromosome 22q11.2 Deletion Syndrome Diagnosed in 12-Year-Old Boys with Hypocalcemic Seizures
por: Hyun, Jae Won, et al.
Publicado: (2012)

Features of Two Cases with 18q Deletion Syndrome
por: Özsu, Elif, et al.
Publicado: (2014)

Myelodysplastic Syndrome with 6q Deletion as the Sole Chromosome Abnormality in an Iranian Patient: A Case Report with Review of Literature
por: Ferdowsi, Shirin, et al.
Publicado: (2013)

Deletion mapping of chromosome 16q in hepatocellular carcinoma
por: Piao, Z, et al.
Publicado: (1999)

FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
por: Panagopoulos, Ioannis, et al.
Publicado: (2017)

Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3
por: Rye, Marie S, et al.
Publicado: (2014)

Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature
por: Goyal, Chanan, et al.
Publicado: (2021)

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome
por: Shapiro, Heather M., et al.
Publicado: (2014)

Distal Deletion of Chromosome 11q Encompassing Jacobsen Syndrome without Platelet Abnormality
por: Sheth, Frenny J, et al.
Publicado: (2014)

Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome Associated with Deletion of Chromosome 20q
por: Manthri, Sukesh, et al.
Publicado: (2018)

Atrial septal defect can be easily missed in chromosome 18q deletion syndrome
por: Sabouni, Mouhamed Amr, et al.
Publicado: (2018)

Case Report: Autoimmune Psychosis in Chromosome 22q11.2 Deletion Syndrome
por: Ciano-Petersen, Nicolás Lundahl, et al.
Publicado: (2021)

Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature
por: Xie, Xiaolei, et al.
Publicado: (2022)

Prenatal diagnosis of a terminal chromosome 1 (q42-q44) deletion: original case report and review of the literature
por: Van Linthout, C, et al.
Publicado: (2016)

A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review
por: Almuzzaini, Bader, et al.
Publicado: (2020)

Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome
por: Colarusso, Gloria, et al.
Publicado: (2010)

PB1912: MYELODYSPLASTIC SYNDROME WITH ISOLATED 5Q DELETION AND ASSOCIATED 5Q DELETION TO 13Q DELETION
por: Bouayed Abdelmoula, N., et al.
Publicado: (2022)

Phosphatase and tensin homologue deleted on chromosome 10
por: Abdulkareem, Imran Haruna, et al.
Publicado: (2013)

Deletion Mapping of Chromosome 10 in Human Glioma
por: Sonoda, Yukihiko, et al.
Publicado: (1996)

Deletion Mapping of Chromosome 1p and 22q in Pheochromocytoma
por: Shin, Eisei, et al.
Publicado: (1993)

Chromosome r(10)(p15.3q26.12) in a newborn child: case report
por: Gunnarsson, Cecilia, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_ckriqjmrsbgmsv5m17dp76lgff