Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report

Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report

Abstract Small supernumerary marker chromosomes (sSMC) can form small supernumerary ring chromosomes (sSRC). Loss of parentally inherited sSRC containing vital gene content may cause an “unbalanced” karyotype and fetal microdeletion syndromes. Rarely, sSRC with neocentromere can be inherited, leadin...

Full description

Bibliographic Details
Main Authors:	Yiming Wang, Joanna Lazier, Diane Myles‐Reid, Abdul Noor, David Chitayat, Elena Greenfeld
Format:	Article
Language:	English
Published:	Wiley 2023-04-01
Series:	Clinical Case Reports
Subjects:	microdeletion neocentromere preimplantation genetic testing small supernumerary ring chromosome
Online Access:	https://doi.org/10.1002/ccr3.6632

Similar Items

Centromere deletion in Cryptococcus deuterogattii leads to neocentromere formation and chromosome fusions
by: Klaas Schotanus, et al.
Published: (2020-04-01)

Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromere
by: Liselot van der Laan, et al.
Published: (2023-11-01)

Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization
by: Pietro Cignini, et al.
Published: (2011-09-01)

Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism
by: M. P. Navarrete-Meneses, et al.
Published: (2024-04-01)

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
by: Chih-Ping Chen, et al.
Published: (2017-04-01)

Massive expansion of sex-specific SNPs, transposon-related elements, and neocentromere formation shape the young W-chromosome from the mosquitofish Gambusia affinis
by: Stefan Müller, et al.
Published: (2023-05-01)

Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl
by: Avinash V. Dharmadhikari, et al.
Published: (2022-07-01)

Molecular Cytogenetics in the Era of Chromosomics and Cytogenomic Approaches
by: Thomas Liehr
Published: (2021-10-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
by: Chih-Ping Chen, et al.
Published: (2011-06-01)

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
by: Igor N. Lebedev, et al.
Published: (2021-08-01)

Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
by: Yang Yang, et al.
Published: (2023-09-01)

First case of two supernumerary markers derived from chromosome 5 and chromosome 8
by: Roberta Giansante, et al.
Published: (2022-06-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2
by: Chih-Ping Chen, et al.
Published: (2017-04-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
by: Chih-Ping Chen, et al.
Published: (2017-06-01)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities
by: Chih-Ping Chen, et al.
Published: (2016-12-01)

Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies
by: Qiping Hu, et al.
Published: (2018-02-01)

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome
by: Chih-Ping Chen, et al.
Published: (2021-01-01)

Editorial: Cytogenomics: Structural Organization and Evolution of Genomes
by: Ricardo Utsunomia, et al.
Published: (2022-06-01)

Mimicking Hypoxic-Ischemic Encephalopathy in a Newborn with 21q Deletion Originating from Ring Chromosome 21
by: Ja Un Moon, et al.
Published: (2023-08-01)

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8
by: Chih-Ping Chen, et al.
Published: (2010-12-01)

Analysis of Y Chromosome Microdeletion in Indonesian Males
by: Dwi Anita Suryandari, et al.
Published: (2010-10-01)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
by: Chih-Ping Chen, et al.
Published: (2016-12-01)

Extraordinary centromeres: differences in the meiotic chromosomes of two rock lizards species Darevskia portschinskii and Darevskia raddei
by: Victor Spangenberg, et al.
Published: (2019-01-01)

Editorial: Co-occurrence of numerical and structural aberration—small supernumerary marker chromosomes and B-chromosomes
by: Thomas Liehr
Published: (2024-04-01)

Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis
by: Huili Xue, et al.
Published: (2019-03-01)

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated With a Reciprocal Translocation Involving Chromosomes 17 And 18
by: Chih-Ping Chen, et al.
Published: (2010-06-01)

Screening Y Chromosome Microdeletion in 1121 Men with Low Sperm Concentration and the Outcomes of Microdissection Testicular Sperm Extraction (mTESE) for Sperm Retrieval from Azoospermic Patients
by: The Trinh S, et al.
Published: (2023-08-01)

Loss of PWT7, Located on a Supernumerary Chromosome, Is Associated with Parasitic Specialization of Pyricularia oryzae on Wheat
by: Soichiro Asuke, et al.
Published: (2023-11-01)

Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes
by: Tingting Li, et al.
Published: (2020-07-01)

Trisomy 21 with a Small Supernumerary Marker Chromosome Derived from Chromosomes 13/21 and 18
by: Niksic S, et al.
Published: (2010-01-01)

Supernumerary Marker Chromosome Identified in Asian Elephant (<i>Elephas maximus</i>)
by: Halina Cernohorska, et al.
Published: (2023-02-01)

Small supernumerary marker chromosomes derived from human chromosome 11
by: Thomas Liehr, et al.
Published: (2023-12-01)

Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
by: María Teresa Alejandra González-Rodríguez, et al.
Published: (2023-01-01)

Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report
by: H. C. Manju, et al.
Published: (2022-03-01)

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report
by: Mohammad Yahya VAHIDI MEHRJARDI, et al.
Published: (2016-03-01)

Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array
by: Lili Zhou, et al.
Published: (2020-05-01)

Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
by: Tatyana V. Karamysheva, et al.
Published: (2020-12-01)

Histone H3K9 and H4 Acetylations and Transcription Facilitate the Initial CENP-AHCP−3 Deposition and De Novo Centromere Establishment in Caenorhabditis elegans Artificial Chromosomes
by: Jing Zhu, et al.
Published: (2018-04-01)

Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)
by: Chih-Ping Chen, et al.
Published: (2022-01-01)

Y chromosome microdeletions in sperm DNA of infertile patients from Tamil Nadu, south India
by: Poongothai J Sakthivel, et al.
Published: (2008-01-01)