Cargando…

Oral Characteristics of Trisomy 8 and Monosomy 18: A Case Report

Several reports described various mosaic chromosomal syndromes characterized by alterations originated by either an excess or deficit in the number of chromosomes. A case of mosaic trisomy 8 and monosomy 18 with significant involvement of the oral cavity is described, both in terms of general medici...

Descripción completa

Detalles Bibliográficos
Autores principales:	Spano, Giovanni, Sale, Silvana, Campus, Guglielmo, Lugliè, Pierfranca
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bentham Open 2011
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162190/ https://www.ncbi.nlm.nih.gov/pubmed/21892366 http://dx.doi.org/10.2174/1874210601105010136

Ejemplares similares

Risk factors for oral mucositis in paediatric oncology patients receiving alkylant chemotherapy
por: Fadda, Giulia, et al.
Publicado: (2006)

The impact of monosomies, trisomies and segmental aneuploidies on chromosomal stability
por: Hintzen, Dorine C., et al.
Publicado: (2022)

Monosomy 18p
por: Turleau, Catherine
Publicado: (2008)

Prenatal Diagnosis of a De Novo Partial Trisomy 6q and Partial Monosomy 18p Associated with Cephalocele: A Case Report
por: Karaman, A, et al.
Publicado: (2020)

Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report
por: Yue, Fagui, et al.
Publicado: (2019)

Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
por: Papadopoulou, Zoe, et al.
Publicado: (2017)

A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy X
por: Demko, Zachary, et al.
Publicado: (2022)

Spontaneous remission of acute monocytic leukemia with trisomy 8 and trisomy 18
por: Suyama, Takahiro, et al.
Publicado: (2019)

Prenatal Diagnosis and Postnatal Followup of Partial Trisomy 13q and Partial Monosomy 10p: A Case Report and Review of the Literature
por: Wei, Yuan, et al.
Publicado: (2012)

Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report
por: Li, Rui, et al.
Publicado: (2023)

Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature
por: Brooks, Brian P, et al.
Publicado: (2006)

Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report
por: Xie, Hui-Hui, et al.
Publicado: (2021)

Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q
por: Zhang, Shuang, et al.
Publicado: (2023)

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination
por: Peterman, Leia A., et al.
Publicado: (2020)

Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
por: Schuy, Jakob, et al.
Publicado: (2022)

Monosomy 21 Seen in Live Born Is Unlikely to Represent True Monosomy 21: A Case Report and Review of the Literature
por: Burgess, Trent, et al.
Publicado: (2014)

The trisomy 18 syndrome
por: Cereda, Anna, et al.
Publicado: (2012)

Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
por: Al Achkar, Walid, et al.
Publicado: (2010)

Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region
por: Brault, Véronique, et al.
Publicado: (2015)

Candidate Genes Associated With Neurological Findings in a Patient With Trisomy 4p16.3 and Monosomy 5p15.2
por: Corrêa, Thiago, et al.
Publicado: (2020)

An efficient method for noninvasive prenatal diagnosis of fetal trisomy 13, trisomy 18, and trisomy 21
por: Sun, Xiaohan, et al.
Publicado: (2019)

Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population
por: Zhuang, Jianlong, et al.
Publicado: (2022)

West syndrome associated with a novel chromosomal anomaly; partial trisomy 8P together with partial monosomy 9P, resulting from a familial unbalanced reciprocal translocation
por: Erol, Ilknur, et al.
Publicado: (2015)

Misdiagnosis of trisomy 13 and trisomy 18 is more common than anticipated
por: Geddes, Gabrielle C., et al.
Publicado: (2022)

Cardiac surgery in children with trisomy 13 or trisomy 18: How safe is it?
por: Rosenblum, Joshua M., et al.
Publicado: (2022)

Congenital hydrocephalus in an Egyptian baby with trisomy 18: a case report
por: Metwalley, Kotb A, et al.
Publicado: (2009)

Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis: Three case reports
por: Qi, Hong, et al.
Publicado: (2019)

Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up
por: Meloni, Vera Ayres, et al.
Publicado: (2014)

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma
por: Gekas, Jean, et al.
Publicado: (2014)

The natural history of pregnancies with a diagnosis of Trisomy 18 or Trisomy 13; a retrospective case series
por: Houlihan, Orla A, et al.
Publicado: (2013)

Are distinctive risk indicators associated with different stages of caries in children? A cross-sectional study
por: Cagetti, Maria Grazia, et al.
Publicado: (2016)

Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
por: Cervantes, Alicia, et al.
Publicado: (2014)

Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
por: Ahn, Jun Mo, et al.
Publicado: (2003)

Small Choroidal Melanoma with Monosomy 3
por: Ghassemi, Fariba, et al.
Publicado: (2010)

Employ ductus venous blood flow in the early detection of trisomy 21, trisomy 18, and trisomy 13: A meta-analysis
por: Ge, Yibing, et al.
Publicado: (2019)

A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3
por: Al Achkar, Walid, et al.
Publicado: (2010)

A Rare Association of Monosomy 18p Syndrome and Polyglandular Autoimmune Syndrome Type IIIA
por: Dolek-Cetinkaya, D, et al.
Publicado: ( 201)

Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype
por: Marinescu, Ponnila S, et al.
Publicado: (2015)

Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies
por: Zhang, Jingbo, et al.
Publicado: (2020)

A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies
por: Joynt, Alyssa C. M., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_k3l8rb60e27n16ks2pv60t0h7u