Literature DB >> 26788866

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.

Erkan Sari1, Abdullah Bereket2, Ediz Yeşilkaya1, Firdevs Baş3, Rüveyde Bundak3, Banu Küçükemre Aydın3, Şükran Darcan4, Bumin Dündar5, Muammer Büyükinan6, Cengiz Kara7, Erdal Adal8, Ayşehan Akıncı9, Mehmet Emre Atabek10, Fatma Demirel11, Nurullah Çelik12, Behzat Özkan13, Bayram Özhan14, Zerrin Orbak15, Betül Ersoy16, Murat Doğan17, Ali Ataş18, Serap Turan2, Damla Gökşen4, Ömer Tarım19, Bilgin Yüksel20, Oya Ercan21, Şükrü Hatun22, Enver Şimşek23, Ayşenur Ökten24, Ayhan Abacı25, Hakan Döneray15, Mehmet Nuri Özbek26, Mehmet Keskin27, Hasan Önal8, Nesibe Akyürek10, Kezban Bulan17, Derya Tepe11, Hamdi Cihan Emeksiz12, Korcan Demir13, Deniz Kızılay16, Ali Kemal Topaloğlu20, Erdal Eren19, Samim Özen4, Hüseyin Demirbilek26, Saygın Abalı2, Leyla Akın8, Beray Selver Eklioğlu10, Sultan Kaba17, Ahmet Anık25, Serpil Baş2, Tolga Unuvar8, Halil Sağlam19, Semih Bolu28, Tolga Özgen8, Durmuş Doğan19, Esra Deniz Çakır19, Yaşar Şen29, Nesibe Andıran11,30, Filiz Çizmecioğlu22, Olcay Evliyaoğlu21, Gülay Karagüzel24, Özgür Pirgon31, Gönül Çatlı25, Hatice Dilek Can19, Fatih Gürbüz20, Çiğdem Binay23, Veysel Nijat Baş32, Kürşat Fidancı1, Davut Gül1, Adem Polat1, Cengizhan Acıkel1, Peyami Cinaz12, Feyza Darendeliler3.   

Abstract

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 1.3 cm shorter and mean birth weight was 0.36 kg 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.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  anthropometry; karyotype; turner syndrome

Mesh:

Year:  2016        PMID: 26788866     DOI: 10.1002/ajmg.a.37498

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Delayed Presentation of Turner Syndrome: Challenge to Optimal Management.

Authors:  Uma Kaimal Saikia; Dipti Sarma; Yogesh Yadav
Journal:  J Hum Reprod Sci       Date:  2017 Oct-Dec

Review 2.  Diagnostic and therapeutic considerations in Turner syndrome.

Authors:  Seung Yang
Journal:  Ann Pediatr Endocrinol Metab       Date:  2017-12-31

3.  Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features

Authors:  Nataliya Zelinska; Iryna Shevchenko; Evgenia Globa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2018-02-28
  3 in total

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