BIOMAT Database Logo BIOMAT Database Logo

[XX-XO-XXS-XS-XX?i mosaicism in a female patient with Turner's syndrome]. 1968

P Fischer, and E Golob, and E Kunze-Mühl

UI MeSH Term Description Entries
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D009030 Mosaicism The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote.
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D004392 Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. Nanism
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
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
D000568 Amenorrhea Absence of menstruation. Postpartum Amenorrhea,Amenorrhea, Postpartum,Postpartum Amenorrheas
D012730 Sex Chromosomes The homologous chromosomes that are dissimilar in the heterogametic sex. There are the X CHROMOSOME, the Y CHROMOSOME, and the W, Z chromosomes (in animals in which the female is the heterogametic sex (the silkworm moth Bombyx mori, for example)). In such cases the W chromosome is the female-determining and the male is ZZ. (From King & Stansfield, A Dictionary of Genetics, 4th ed) Gonosomes,Chromosome, Sex,Chromosomes, Sex,Gonosome,Sex Chromosome
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

P Fischer, and E Golob, and E Kunze-Mühl
[XY, XO, XX mosaicism with Turner's syndrome].
January 1967, Bulletin de la Federation des societes de gynecologie et dobstetrique de langue francaise,
P Fischer, and E Golob, and E Kunze-Mühl
[Metabolism and growth hormone in female patients with non-typical Turner's syndrome (XO-XX-XXX mosaicism; XO-XX mosaicism)].
March 1969, Monatsschrift fur Kinderheilkunde,
P Fischer, and E Golob, and E Kunze-Mühl
TURNER'S SYNDROME WITH XO-XX MOSAICISM. A CASE PRESENTATION.
June 1964, Henry Ford Hospital medical bulletin,
P Fischer, and E Golob, and E Kunze-Mühl
Turner's syndrome with XO-XX mosaicism and normal puberty.
December 1971, The Journal of pediatrics,
P Fischer, and E Golob, and E Kunze-Mühl
[XO-XY mosaicism in a female phenotype with Turner's syndrome].
August 1970, Vnitrni lekarstvi,
P Fischer, and E Golob, and E Kunze-Mühl
[Congenital lymphedema and Turner's syndrome. 2 cases with XX-XO mosaicism].
January 1971, Annales de pediatrie,
P Fischer, and E Golob, and E Kunze-Mühl
[TURNER'S SYNDROME WITH XX/XO KARYOTYPE].
March 1964, Archives francaises de pediatrie,
P Fischer, and E Golob, and E Kunze-Mühl
Down syndrome with XO/XX mosaicism.
January 1979, Acta paediatrica Academiae Scientiarum Hungaricae,
P Fischer, and E Golob, and E Kunze-Mühl
[Clinical difference between XO Turner's syndrome and 45,X-46,XX mosaicism].
March 1970, Jinrui idengaku zasshi. The Japanese journal of human genetics,
P Fischer, and E Golob, and E Kunze-Mühl
[Polyneuropathy in a patient with Turner's mosaicism 45(XO)-46(XX) and hexobarbital abuse for years].
January 1972, Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete,
Copied contents to your clipboard!