+15 or trisomy 15 (as sole autosomal abnormality)
نویسندگان
چکیده
منابع مشابه
Trisomy Chromosome 6 as a Sole Cytogenetic Abnormality in Acute Myeloid Leukemia
Identification of cytogenetic abnormalities plays an important role in the diagnosis and prognosis of leukemias. Isolated trisomy 6 is a rare abnormality, the prognostic significance of which is not well established. We report one case of acute myeloid leukemia (AML-M5 variant) with trisomy 6 as the sole cytogenetic abnormality. Previously, trisomy 6 has been reported in aplastic anemia, myelod...
متن کاملAcute myeloid leucaemia with trisomy 14 as a sole cytogenetic abnormality.
To cite: Reserva J, Loleng M, Marchalik R, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015212552 DESCRIPTION Trisomy 14 as a sole cytogenetic abnormality is a rare non-random recurrent change that has been reported in myeloid neoplasms. We report a case of an elderly patient with medical history of coronary artery disease who presented to the emergency...
متن کاملTrisomy 15 mosaicism in an IVF fetus.
Prenatal diagnosis of an IVF pregnancy in a woman aged 41 years showed a fetus mosaic for trisomy 15. The fetus had dysmorphic features, hypoplastic adrenal glands, and an accessory spleen. Both IVF and advanced maternal age would seem to increase the risk of trisomy 15.
متن کاملThe inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
The inv dup(15) or idic(15) syndrome displays distinctive clinical findings represented by early central hypotonia, developmental delay and intellectual disability, epilepsy, and autistic behaviour. Incidence at birth is estimated at 1 in 30,000 with a sex ratio of almost 1:1. Developmental delay and intellectual disability affect all individuals with inv dup(15) and are usually moderate to pro...
متن کاملNormal-trisomy 13-15 Mosaicism in Two Infants.
It is generally accepted that there is a recognizable clinical syndrome associated with trisomy for one of the 13-15 group of chromosomes. The clinical features of this trisomic syndrome were first described by Patau, Smith, Therman, Inhorn, and Wagner (1960). In a recent paper Smith, Patau, Therman, Inhorn, and DeMars (1963) described a series of 7 cases and reviewed 7 others. The majority of ...
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ژورنال
عنوان ژورنال: Atlas of Genetics and Cytogenetics in Oncology and Haematology
سال: 2011
ISSN: 1768-3262
DOI: 10.4267/2042/37517