Articles on Turner Syndrome

AYNUR ACAR, İBRAHIM ERKUL, SENNUR DEMIREL, HASAN ACAR, TÜLİN ÇORA, SAID GÖNEN

1990, Vol 6, Issue 3, Page 315-319

A 12 years old fernak case who was one of the twin sisters and the other 20 years old female case with growth deficiency and lack of menstrual period were referred to our laboratory for possible Turner Syndrome. The first case whose twin sister had normal growth and development with 46, XX...

MEHMET EMRE ATABEK, BÜLENT ORAN, İBRAHIM ERKUL, AYŞEGÜL ZAMANİ, AYNUR ACAR

1999, Vol 15, Issue 4, Page 227-229

The work presents the clinical and cytogenetic findings in a 8 year-old female-patient with Turner phenotype and 46,X,del(X)(q22) karyotype. We discuss the difficulties of phenotype -karyotype correlation in cases with X chromosome structural aberation.

AYŞEGÜL ZAMANİ, SENNUR DEMIREL, HATİCE GÜL DURSUN, TÜLİN ÇORA, AYNUR ACAR

2002, Vol 18, Issue 1, Page 5-8

Cytogenetic analysis of 37 patients, who were referred to our laboratory because of primary amenorrhea ,growth retardation and Turner's syndrome stigmata were performed and X chromosome abnormalities were evaluated. Monosomi X constituted approximately half of our patients(48,6%).Mosaic karyotypes...

TALAT YURDAKUL, OKAN MUSTAFA İSTANBULLUOĞLU, MEHMET MESUT PİŞKİN

2002, Vol 18, Issue 2, Page 123-126

Horseshoe kidney is the most common type of renal fusion malformation. The incidence rate is % 0.25 İn public. This malformation may accompany to the chromosomal abnormalities. The most freguent renal abnormality in Turner syndrome is horseshoe kidney. There might be seen complications such as...