Page last updated: 2024-10-20

spermine and Turner Syndrome

spermine has been researched along with Turner Syndrome in 1 studies

Turner Syndrome: A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rudman, D1
Kutner, MH1
Chawla, RK1
Goldsmith, MA1
Blackston, RD1
Bain, R1

Other Studies

1 other study available for spermine and Turner Syndrome

ArticleYear
Serum and urine polyamines in normal and in short children.
    The Journal of clinical investigation, 1979, Volume: 64, Issue:6

    Topics: Adolescent; Adult; Age Factors; Aged; Child; Dwarfism; Female; Growth Disorders; Growth Hormone; Hum

1979