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Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome
American Journal of Medical Genetics Part A 2016 Cilt 170 Sayı 4
Scopus Eşleşmesi Bulundu
11
Atıf
170
Cilt
942-948
Sayfa
Özet
To evaluate the anthropometric features of girls with Turner syndrome (TS) at birth and presentation and the effect of karyotype on these parameters. Data were collected from 842 patients with TS from 35 different centers, who were followed-up between 1984 and 2014 and whose diagnosis age ranged from birth to 18 years. Of the 842 patients, 122 girls who received growth hormone, estrogen or oxandrolone were excluded, and 720 girls were included in the study. In this cohort, the frequency of small for gestational age (SGA) birth was 33%. The frequency of SGA birth was 4.2% (2/48) in preterm and 36% (174/483) in term neonates (P<0.001). The mean birth length was 1.3cm shorter and mean birth weight was 0.36kg lower than that of the normal population. The mean age at diagnosis was 10.1±4.4 years. Mean height, weight and body mass index standard deviation scores at presentation were -3.1±1.7, -1.4±1.5, and 0.4±1.7, respectively. Patients with isochromosome Xq were significantly heavier than those with other karyotype groups (P=0.007). Age at presentation was negatively correlated and mid-parental height was positively correlated with height at presentation. Mid-parental height and age at presentation were the only parameters that were associated with height of children with TS. The frequency of SGA birth was found higher in preterm than term neonates but the mechanism could not be clarified. We found no effect of karyotype on height of girls with TS, whereas weight was greater in 46,X,i(Xq) and 45,X/46,X,i(Xq) karyotype groups.

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Scimago Dergi Bilgisi Otomatik ISSN Eşleştirmesi 2016 yılı verileri
American Journal of Medical Genetics, Part A
Q2
SJR Quartile
1,171
SJR Skoru
136
H-Index
Kategoriler: Genetics (Q2) · Genetics (clinical) (Q3)
Alanlar: Biochemistry, Genetics and Molecular Biology · Medicine
Ülke: United States · John Wiley and Sons Inc
Bu bilgiler makale yılına göre Scimago veritabanından ISSN eşleştirmesiyle otomatik getirilmektedir. Dergi sıralama verileri Scimago'nun ilgili yılı baz alınmaktadır.

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Makale Bilgileri

Dergi American Journal of Medical Genetics Part A
ISSN 1552-4825
Yıl 2016 / 4. ay
Cilt / Sayı 170 / 4
Sayfalar 942 – 948
Makale Türü Özgün Makale
Hakemlik Hakemli
Endeks SCI-Expanded
Yayın Dili İngilizce
Kapsam Uluslararası
Toplam Yazar 73 kişi
Erişim Türü Elektronik
Alan Sağlık Bilimleri Temel Alanı Çocuk Endokrinolojisi

YÖKSİS Yazar Kaydı

Yazar Adı SARI ERKAN, BEREKET ABDULLAH, YEŞİLKAYA EDİZ, BAŞ FİRDEVS, BUNDAK RÜVEYDE, KÜÇÜKEMRE AYDIN BANU, DARCAN ŞÜKRAN, DÜNDAR BUMİN NURİ, BÜYÜKİNAN MUAMMER, KARA CENGİZ, ADAL ERDAL, AKINCI AYŞEHAN, ATABEK MEHMET EMRE, DEMİREL FATMA, ÇELİK NURULLAH, ÖZKAN BEHZAT, ÖZHAN BAYRAM, ORBAK ZERRİN, ERSOY BETÜL, DOĞAN MURAT, TEPE DERYA
YÖKSİS ID 5708315

Metrikler

Scopus Atıf 11
Havuz Atıfları 0
Yazar Sayısı 73