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A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion.

Authors :
Yıldırım Ş
Topaloğlu N
Tekin M
Sılan F
Source :
Acta medica Iranica [Acta Med Iran] 2017 Oct; Vol. 55 (10), pp. 661-663.
Publication Year :
2017

Abstract

We report a case of 11-year-old girl with growth retardation and 46, XX, Xq27-qter deletion. The endocrinologic evaluation revealed growth hormone deficiency. In karyotype analysis  46, XX, Xq27-qter deletion was determined. The deletion of terminal region of chromosome 27 is most commonly being detected during the evaluation of infertility, premature ovarian insufficiency or in screening for fragile X carrier status. To our knowledge, this is the first reported case with 46, XX, Xq27-qter deletion and growth hormone deficiency. Furthermore, this case might facilitate future search for candidate genes involved in growth hormone deficiency.

Details

Language :
English
ISSN :
1735-9694
Volume :
55
Issue :
10
Database :
MEDLINE
Journal :
Acta medica Iranica
Publication Type :
Academic Journal
Accession number :
29228534