[Congenital somatic anomalies in gonadal dysgenesis syndrome]. 1972

A Galazka, and H Glebowska, and I Orelska

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D001724 Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. Birthweight,Birth Weights,Birthweights,Weight, Birth,Weights, Birth
D001827 Body Height The distance from the sole to the crown of the head with body standing on a flat surface and fully extended. Body Heights,Height, Body,Heights, Body
D001835 Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. Body Weights,Weight, Body,Weights, Body
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D014424 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. Bonnevie-Ullrich Syndrome,Gonadal Dysgenesis, 45,X,Gonadal Dysgenesis, XO,Monosomy X,Status Bonnevie-Ullrich,Turner's Syndrome,Ullrich-Turner Syndrome,Bonnevie Ullrich Syndrome,Status Bonnevie Ullrich,Syndrome, Ullrich-Turner,Turners Syndrome,Ullrich Turner Syndrome,XO Gonadal Dysgenesis

Related Publications

A Galazka, and H Glebowska, and I Orelska
June 1960, The American journal of medicine,
A Galazka, and H Glebowska, and I Orelska
May 2015, Fertility and sterility,
A Galazka, and H Glebowska, and I Orelska
October 1965, The American journal of roentgenology, radium therapy, and nuclear medicine,
A Galazka, and H Glebowska, and I Orelska
April 1966, Rassegna di neurologia vegetativa,
A Galazka, and H Glebowska, and I Orelska
December 2016, Clinical nephrology,
A Galazka, and H Glebowska, and I Orelska
March 1980, Obstetrics and gynecology,
A Galazka, and H Glebowska, and I Orelska
February 1983, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae,
A Galazka, and H Glebowska, and I Orelska
March 1985, Chinese medical journal,
A Galazka, and H Glebowska, and I Orelska
March 1963, Dapim refuiim. Folia medica,
A Galazka, and H Glebowska, and I Orelska
January 1966, Radiology,
Copied contents to your clipboard!