نتایج جستجو برای: partial trisomy 22

تعداد نتایج: 439803  

Journal: :Journal of medical genetics 1978
S H Roberts D P Duckett

An abnormal female infant, who survived for 10 months with almost complete trisomy 16p and monosomy of sub-band 21q22.3, is described. The chromosome anomaly was the result of an unbalanced segregation of a maternal balanced translocation t(16;21)(p11;q22.3). The partial monosomy was considered to have had little or no adverse phenotypic effect. Cases with trisomy of chromosome 16 material are ...

Journal: :Blood 2013
Peter Paschka Juan Du Richard F Schlenk Verena I Gaidzik Lars Bullinger Andrea Corbacioglu Daniela Späth Sabine Kayser Brigitte Schlegelberger Jürgen Krauter Arnold Ganser Claus-Henning Köhne Gerhard Held Marie von Lilienfeld-Toal Heinz Kirchen Mathias Rummel Katharina Götze Heinz-August Horst Mark Ringhoffer Michael Lübbert Mohammed Wattad Helmut R Salih Andrea Kündgen Hartmut Döhner Konstanze Döhner

In this study, we evaluated the impact of secondary genetic lesions in acute myeloid leukemia (AML) with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11. We studied 176 patients, all enrolled on prospective treatment trials, for secondary chromosomal aberrations and mutations in N-/KRAS, KIT, FLT3, and JAK2 (V617F) genes. Most frequent chromosomal aberrations were trisomy 22 (18%) and tris...

Journal: :Journal of Korean Medical Science 1992
C. J. Kim J. G. Chi K. H. Lee C. K. Lee M. S. Yoo Y. K. Paik

The authors describe a male newborn with multiple congenital anomalies; craniofacial dysmorphism, bilateral cleft palate and lip, ambiguous external genitalia with absence of phallus, ventricular septal defect, agenesis of olfactory bulbs, and presence of small round cells simulating migration defect in the cerebellar white matter. Cytogenetic study demonstrated a chromosomal constitution of 47...

Journal: :Haematologica 2007
Ayami Yoshimi Irith Baumann Monika Führer Eva Bergsträsser Ulrich Göbel Karl-Walter Sykora Thomas Klingebiel Ute Gross-Wieltsch Marry M van den Heuvel-Eibrink Alexandra Fischer Peter Nöllke Charlotte Niemeyer

It is currently unknown whether immunosuppressive therapy or hematopoietic stem cell transplantation is the most appropriate treatment strategy for children with refractory cytopenia and normal karyotype or trisomy 8. We report on 31 children with hypoplastic refractory cytopenia treated with immunosuppressive therapy consisting of antithymocyte globulin and cyclosporine. At 6 months, 22 of 29 ...

Journal: :Journal of Medical Genetics 1979

Journal: :Daehan binyogi jong-yang haksulji 2022

Liposarcomas of the spermatic cord are rare and often clinically histologically misdiagnosed, leading to ineffective management poor outcomes. We present a case metastatic dedifferentiated liposarcoma cord, which recurred after excision misdiagnosed well-differentiated 3 years prior. Due its size high-grade metastasis, tumor was unresectable, treatment with systemic chemotherapy. Complications ...

Journal: :Japanese journal of human genetics 1987

Journal: :Development 2005
Karoline J Briegel H Scott Baldwin Jonathan A Epstein Alexandra L Joyner

Partial trisomy 2p syndrome includes a spectrum of congenital heart disease (CHD) that is characterized by complex malformations of the outflow and inflow tracts, defects in cardiac septation, heart position, as well as abnormal ventricular development. Lbh (limb-bud and heart) is a novel, highly conserved putative transcriptional regulatory protein, which displays a unique spatiotemporal gene ...

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