Turner Syndrome D014424

Related MeSH Hierarchy (15)

Diseases [C] » Cardiovascular Diseases [C14] » Cardiovascular Abnormalities » Heart Defects, Congenital » Turner Syndrome

Diseases [C] » Cardiovascular Diseases [C14] » Heart Diseases » Heart Defects, Congenital » Turner Syndrome

Description

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.   MeSH

Approved Indicated Drugs (2)

Phase 4 Indicated Drugs (2)

Phase 2 Indicated Drugs (1)

Other Experimental Indicated Drugs (1)


Organization Involved with Other Experimental Indications (3)

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