PREGNANCY AND TURNER SYNDROME
- 1 January 1978
- journal article
- research article
- Vol. 52 (5) , 617-624
Abstract
A 21 yr old white female with short stature, cubitus valgus, multiple cutaneous nevi and no other major features of the Turner syndrome is described. She had normal secondary sex development and menses. She recently completed a normal pregnancy with delivery of a normal male infant. Postpartum endocrine studies were normal. All cells examined from blood, skin, uterus and both ovaries had a 45,X karyotype. She is the 6th reported monosomy X patient to achieve pregnancy. A literature review indicates increased fetal wastage (22 of 46 pregnancies) and increased chromosomal errors in the offspring (8 of 26 liveborn infants) of patients with a 45,X cell line. Three cases of trisomy 21 occurred in these infants. Amniocentesis and prenatal diagnostic studies are indicated for women with a 45,X chromosome constitution. The pathogenesis of the Turner syndrome is considered in relation to these findings.This publication has 6 references indexed in Scilit:
- Fertility in women with gonadal dysgenesisAmerican Journal of Obstetrics and Gynecology, 1976
- A possible active segment on the inactive human X chromosomeChromosoma, 1976
- The anatomy and histology of XO human embryos and fetusesThe Anatomical Record, 1966
- 45/XO Turner's Syndrome in the Newborn: Report of Two CasesJournal of Clinical Endocrinology & Metabolism, 1963
- TURNER-SYNDROM MIT VOLL AUSGEBILDETEN SEKUNDAREN GESCHLECHTSMERKMALEN UND FERTILITAT1960
- A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1Endocrinology, 1938