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Karapinar, Deniz Yilmaz; Patiroglu, Turkan; Metin, Ayse; Caliskan, Umran; Celkan, Tiraje; Yilmaz, Baris; Karakas, Zeynep; Karapinar, Tuba H.; Akinci, Burcu; Ozkinay, Ferda; Onay, Huseyin; Yesilipek, Mehmet Akif; Akar, Himmet Haluk; Tuysuz, Gulen; Tokgoz, Huseyin; Ozdemir, Gul Nihal; Kiykim, Ayca Aslan; Karaman, Serap; Kilinc, Yurdanur; Oymak, Yesim; Oymak, Yesim
<?xml version='1.0' encoding='UTF-8'?> <record xmlns="http://www.loc.gov/MARC21/slim"> <leader>00000nam##2200000uu#4500</leader> <datafield tag="245" ind1=" " ind2=" "> <subfield code="a">Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry</subfield> </datafield> <datafield tag="909" ind1="C" ind2="4"> <subfield code="p">PEDIATRIC BLOOD & CANCER</subfield> <subfield code="v">66</subfield> <subfield code="n">10</subfield> </datafield> <controlfield tag="001">71535</controlfield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="520" ind1=" " ind2=" "> <subfield code="a">Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and Western Europe. However, in eastern countries where consanguineous marriages are common, autosomal recessive forms might be more frequent. Method Two hundred and sixteen patients with severe congenital neutropenia from 28 different pediatric centers in Turkey were registered. Results The most frequently observed mutation was HAX1 mutation (n = 78, 36.1%). A heterozygous ELANE mutation was detected in 29 patients (13.4%) in our cohort. Biallelic mutations of G6PC3 (n = 9, 4.3%), CSF3R (n = 6, 2.9%), and JAGN1 (n = 2, 1%) were also observed. Granulocyte colony-stimulating factor treatment was given to 174 patients (80.6%). Two patients died with infectious complications, and five patients developed myelodysplastic syndrome/acute myeloblastic leukemia. The mean (+/- mean standard error) follow-up period was 129.7 +/- 76.3 months, and overall survival was 96.8% (CI, 94.4-99.1%) at the age of 15 years. In Turkey, severe congenital neutropenia mostly resulted from the p W44X mutation in the HAX1 gene. Conclusion In Turkey, mutation analysis should be started with HAX1, and if this is negative, ELANE and G6PC3 should be checked. Because of the very high percentage of consanguineous marriage, rare mutations should be tested in patients with a negative mutation screen.</subfield> </datafield> <datafield tag="650" ind1="1" ind2="7"> <subfield code="2">opendefinition.org</subfield> <subfield code="a">cc-by</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Erciyes Univ, Fac Med, Dept Pediat Immunol, Izmir, Turkey</subfield> <subfield code="a">Patiroglu, Turkan</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Ankara Childrens Hematol Oncol Training & Res Hos, Dept Pediat Immunol, Ankara, Turkey</subfield> <subfield code="a">Metin, Ayse</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Necmettin Erbakan Univ, Meram Fac Med, Dept Pediat Hematol Oncol, Konya, Turkey</subfield> <subfield code="a">Caliskan, Umran</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Istanbul Univ, Cerrahpasa Med Fac, Dept Pediat Hematol, Istanbul, Turkey</subfield> <subfield code="a">Celkan, Tiraje</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Marmara Univ, Fac Med, Dept Pediat Hematol, Istanbul, Turkey</subfield> <subfield code="a">Yilmaz, Baris</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Istanbul Univ, Istanbul Fac Med, Dept Pediat Hematol Oncol, Istanbul, Turkey</subfield> <subfield code="a">Karakas, Zeynep</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Dr Behcet Uz Children Res & Training Hosp, Dept Pediat Hematol Oncol, Izmir, Turkey</subfield> <subfield code="a">Karapinar, Tuba H.</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Ege Univ, Fac Med, Dept Pediat Hematol, Izmir, Turkey</subfield> <subfield code="a">Akinci, Burcu</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Ege Univ, Fac Med, Dept Pediat Genet, Izmir, Turkey</subfield> <subfield code="a">Ozkinay, Ferda</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Ege Univ, Fac Med, Dept Med Genet, Izmir, Turkey</subfield> <subfield code="a">Onay, Huseyin</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Med Pk Goztepe Hosp, Pediat Bone Marrow Transplantat Unit, Istanbul, Turkey</subfield> <subfield code="a">Yesilipek, Mehmet Akif</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Erciyes Univ, Fac Med, Dept Pediat Immunol, Izmir, Turkey</subfield> <subfield code="a">Akar, Himmet Haluk</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Akdeniz Univ, Med Sch, Dept Pediat Hematol, Antalya, Turkey</subfield> <subfield code="a">Tuysuz, Gulen</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Necmettin Erbakan Univ, Meram Fac Med, Dept Pediat Hematol Oncol, Konya, Turkey</subfield> <subfield code="a">Tokgoz, Huseyin</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Istanbul Univ, Cerrahpasa Med Fac, Dept Pediat Hematol, Istanbul, Turkey</subfield> <subfield code="a">Ozdemir, Gul Nihal</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Marmara Univ, Fac Med, Dept Pediat Allergy & Immunol, Istanbul, Turkey</subfield> <subfield code="a">Kiykim, Ayca Aslan</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Istanbul Univ, Istanbul Fac Med, Dept Pediat Hematol Oncol, Istanbul, Turkey</subfield> <subfield code="a">Karaman, Serap</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Cukurova Univ, Fac Med, Dept Pediat Hematol, Adana, Turkey</subfield> <subfield code="a">Kilinc, Yurdanur</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Dr Behcet Uz Children Res & Training Hosp, Dept Pediat Hematol Oncol, Izmir, Turkey</subfield> <subfield code="a">Oymak, Yesim</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="u">Dr Behcet Uz Children Res & Training Hosp, Dept Pediat Hematol Oncol, Izmir, Turkey</subfield> <subfield code="a">Oymak, Yesim</subfield> </datafield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="b">article</subfield> <subfield code="a">publication</subfield> </datafield> <datafield tag="542" ind1=" " ind2=" "> <subfield code="l">open</subfield> </datafield> <datafield tag="100" ind1=" " ind2=" "> <subfield code="u">Ege Univ, Fac Med, Dept Pediat Hematol, Izmir, Turkey</subfield> <subfield code="a">Karapinar, Deniz Yilmaz</subfield> </datafield> <datafield tag="260" ind1=" " ind2=" "> <subfield code="c">2019-01-01</subfield> </datafield> <controlfield tag="005">20210316033025.0</controlfield> <datafield tag="909" ind1="C" ind2="O"> <subfield code="o">oai:zenodo.org:71535</subfield> <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="856" ind1="4" ind2=" "> <subfield code="z">md5:863c04c421393c08286d054953a5045e</subfield> <subfield code="s">481</subfield> <subfield code="u">https://aperta.ulakbim.gov.trrecord/71535/files/bib-9c277617-d17e-4338-abc9-a5e018ab2f29.txt</subfield> </datafield> <datafield tag="540" ind1=" " ind2=" "> <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield> <subfield code="a">Creative Commons Attribution</subfield> </datafield> <datafield tag="024" ind1=" " ind2=" "> <subfield code="a">10.1002/pbc.27923</subfield> <subfield code="2">doi</subfield> </datafield> </record>
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