نتایج جستجو برای: tetrasomy

تعداد نتایج: 240  

2017
Javad Karimzad Hagh Thomas Liehr Hamid Ghaedi Mir Majid Mossalaeie Shohreh Alimohammadi Faegheh Inanloo Hajiloo Zahra Moeini Sadaf Sarabi Davood Zare-Abdollahi

Small supernumerary marker chromosomes (sSMC) are still a major problem in clinical cytogenetics as they cannot be identified or characterized unambiguously by conventional cytogenetics alone. On the other hand, and perhaps more importantly in prenatal settings, there is a challenging situation for counseling how to predict the risk for an abnormal phenotype, especially in cases with a de novo ...

Journal: :Cytogenetics and cell genetics 2000
B Levy P Papenhausen J Tepperberg T Dunn S Fallet M Magid N Kardon K Hirschhorn P Warburton

Neocentromeres are fully functional centromeres found on rearranged or marker chromosomes that have separated from endogenous centromeres. Neocentromeres often result in partial tri- or tetrasomy because their formation confers mitotic stability to acentric chromosome fragments that would normally be lost. We describe the prenatal identification and characterization of a de novo supernumerary m...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2018

Journal: :Genes, chromosomes & cancer 2007
Nyla A Heerema Susana C Raimondi James R Anderson Jaclyn Biegel Bruce M Camitta Linda D Cooley Paul S Gaynon Betsy Hirsch R Ellen Magenis Loris McGavran Shivanand Patil Mark J Pettenati Jeanette Pullen Kathleen Rao Diane Roulston Nancy R Schneider Jonathan J Shuster Warren Sanger Maxine J Sutcliffe Peter van Tuinen Michael S Watson Andrew J Carroll

Children with acute lymphoblastic leukemia (ALL) and high hyperdiploidy (>50 chromosomes) are considered to have a relatively good prognosis. The specific extra chromosomes are not random; extra copies of some chromosomes occur more frequently than those of others. We examined the extra chromosomes present in high hyperdiploid ALL to determine if there were a relation of the specific extra chro...

Journal: :European journal of medical genetics 2012
Francis M Filloux John C Carey Ian D Krantz Jeffrey J Ekstrand Meghan S Candee

Pallister-Killian syndrome (PKS) is a rare, sporadic genetic disorder caused by tetrasomy 12p mosaicism associated with a supernumerary isochromosome. Craniofacial dysmorphism, learning impairment and seizures are considered characteristic. However, little is known of the seizure and epilepsy patterns seen in PKS. To better define the occurrence and nature of epileptic and non-epileptic paroxys...

Journal: :Maedica 2011
Vasilica Plaiasu Diana Ochiana Gabriela Motei Adrian Georgescu

BACKGROUND Tetrasomy 18p is a very rare chromosomal disorder and is the result of a spontaneous mutation early in embryonic development in most of the cases. This condition is characterised by the presence of a supernumerary 18p isochromosome (i(18p)) in all or some cells of the affected individual. It has a prevalence of 1/180000 live births and affects both genders equally. MATERIALS AND ME...

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