[State of permanent teeth in mixed forms of gonadal dysgenesis]. 1976

Iu A Beliakov, and I G Dzenis

UI MeSH Term Description Entries
D008297 Male Males
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
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
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
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
D018126 Odontodysplasia A localized arrested tooth development which appears to involve most commonly the anterior teeth, usually on one side of the midline, most often the maxillary central and lateral incisors. Roentgenographically, the teeth have a ghostlike appearance. Calcification and bits of prismatic enamel may be found in the pulp and the enamel is thin and absent in part. (Jablonski, Illustrated Dictionary of Dentistry, 1982) Ghost Teeth,Odontogenesis Imperfecta,Odontogenic Dysplasia,Ghost Tooth,Dysplasia, Odontogenic,Dysplasias, Odontogenic,Odontodysplasias,Odontogenic Dysplasias,Teeth, Ghost,Tooth, Ghost

Related Publications

Iu A Beliakov, and I G Dzenis
June 2006, Nihon rinsho. Japanese journal of clinical medicine,
Iu A Beliakov, and I G Dzenis
January 1977, Nihon rinsho. Japanese journal of clinical medicine,
Iu A Beliakov, and I G Dzenis
April 1966, Rassegna di neurologia vegetativa,
Iu A Beliakov, and I G Dzenis
January 1975, Acta endocrinologica. Supplementum,
Iu A Beliakov, and I G Dzenis
January 1966, Annales de genetique,
Iu A Beliakov, and I G Dzenis
January 1993, Ryoikibetsu shokogun shirizu,
Iu A Beliakov, and I G Dzenis
January 1988, Revista chilena de obstetricia y ginecologia,
Iu A Beliakov, and I G Dzenis
January 1969, La Pediatria,
Iu A Beliakov, and I G Dzenis
March 1978, Journal d'urologie et de nephrologie,
Iu A Beliakov, and I G Dzenis
January 1967, Gynaecologia. International monthly review of obstetrics and gynecology. Revue internationale mensuelle d'obstetrique et de gynecologie. Monatsschrift fur Geburtshilfe und Gynakologie,
Copied contents to your clipboard!