Gonadal dysgenesis

46,XY Gonadal Dysgenesis, Complete, SRY-Related: Introduction
46,XY Gonadal Dysgenesis, Complete, SRY-Related: A rare disorder where a female has all the normal external femal characteristics but has non-functioning gonads.

Alternate Names : Bonnevie-Ullrich syndrome, Gonadal dysgenesis, Monosomy X
Definition
Turner syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes.

Turners Syndrome (Bonnevie-Ullrich syndrome; Gonadal dysgenesis; Monosomy X) ...

Gonadal dysgenesis occurs in hermaphroditism, which is rare.
In cryptorchidism, one or both testes are undescended (see Congenital Renal and Genitourinary Anomalies: Cryptorchidism). Etiology is usually unknown.

Gonadal dysgenesis: Children who have internal organs that are primarily female, external genitals that may vary between normal female and normal male and an underdeveloped gonad.

Gonadal dysgenesis - children who have:
an undeveloped gonad.
internal sex organs that are usually female.
external genitals that may vary between normal female and normal male, with the majority female.

Gonadal dysgenesis is the name of a condition in which the ovaries are prematurely depleted of follicles and oocytes (egg cells) leading to premature failure of the ovaries. It is one of the most common cases of primary amenorrhea in young women.

gonadal dysgenesis (goh-NA-dul dis-JEH-neh-sis) Abnormal development of a gonad (ovary or testicle). Men with gonadal dysgenesis have a greater risk of developing testicular cancer. Gonadal dysgenesis is usually part of a genetic syndrome.

Gonadal Dysgenesis (45,X)
Gonadal Dysgenesis (XO)
Gonadal Dysgenesis, XY Female Type
Gonadotropin Treatment for Infertility - Medication
Gonadotropin-Independent Familial Sexual Precocity ...

46, XY Complete Gonadal Dysgenesis
46, XY Pure Gonadal Dysgenesis
47,XXX Chromosome Constitution
47,XXX Karyotype
47,XXX Syndrome
47,XYY Karyotype
47,XYY Syndrome
49, XXXXX Chromosome Constitution
49, XXXXX Karyotype
49,XXXXX Syndrome ...

Gonadal Dysgenesis (45,X)
Gonadal Dysgenesis (XO)
Gonadal Dysgenesis, XY Female Type
Gonadotropin-Independent Familial Sexual Precocity
Goniodysgenesis-Hypodontia
Goniotomy for Glaucoma
Gonococcal Perihepatitis
Gonorrhea
Gonorrheal Proctitis ...

Clinical manifestations and diagnosis of Turner syndrome (gonadal dysgenesis)
Clinical manifestations and evaluation of spontaneous primary ovarian insufficiency (premature ovarian failure)
Clinical manifestations of adrenal insufficiency in adults ...

Mixed gonadal dysgenesis (MGD). An intersex condition in which there appears some male structures (gonad, testis), as well as a uterus, vagina, and fallopian tubes.
Congenital adrenal hyperplasia.

UAL, CSR, Dental Material, Digital Radiography, DNA Repair Methyltransferase I, Foramen, Apical, Gonadal Dysgenesis, 46, XY, Hepatic Neoplasm, HLA-DR1, Holistic Health, Immunoblastic Lymphadenopathy, In-Hospital Mortalities, Infections, ...

Pure gonadal dysgenesis (defective development of the ovary)
Autoimmune oophoritis (cells of the ovaries destroyed by the body’s own defense system)
Fragile X premutation
Radiation or chemotherapy ...

Gonadal dysgenesis
Hypoglycemia
Hypothyroidism and hyperthyroidism
Cystic fibrosis
Cushing's disease
Polycystic ovarian disease
Chromosomal abnormalities such as Turner's syndrome (XO) or Sawyer's syndrome (XY)
Hypogonadotropic hypogonadism ...

Bonnevie-Ullrich syndrome, gonadal dysgenesis, monosomy X, Morgagni-Turner-Albright syndrome, ovarian dwarfism, ovary aplasia, pterygolymphangiectasia, Schereshevkii-Turner syndrome, sex chromosomes, Turner type, Turner-Varny syndrome, ...

: [Pure 46XY gonadal dysgenesis] J Gynecol Obstet Biol Reprod (Paris) 25 (8): 792-6, 1996.
Amice V, Amice J, Bercovici JP, et al.: Gonadal tumor and H-Y antigen in 46,XY pure gonadal dysgenesis. Cancer 57 (7): 1313-7, 1986.
Stage Information ...

Abnormal gonads (due to gonadal dysgenesis and androgen insensitivity syndrome) have a high risk[3] of developing a dysgerminoma.

Bonnevie-Ullrich syndrome; Gonadal dysgenesis; Monosomy X
Definition of Turner syndrome:
Turner syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes.

Gene Review: 46,XY Disorder of Sex Development and 46,XY Complete Gonadal Dysgenesis
Gene Tests: DHH
Gene Tests: NR0B1
Gene Tests: NR5A1
Gene Tests: SRY
MedlinePlus Encyclopedia: Intersex ...

24-Hour Urine Test
45, X Gonadal Dysgenesis (Turner Syndrome)
Featured Centers
- ...

Congenital abnormalities of the upper genital system
Craniopharyngioma
Cystic fibrosis
Gonadal dysgenesis
Prader-Willi syndrome
Testicular feminization syndrome
True hermaphroditism
Turner syndrome (XO) ...

It causes abnormal development of the ovaries (gonadal dysgenesis). Girls with the condition usually don't have periods. Girls or women with Turner syndrome are usually short and have a broad chest, low hairline, low set ears, and webbed necks.

Urogenital Imaging
Agenesis, ovarian
see gonadal dysgenesis and Turners syndrome
HH ...

Adrenal tumour during pregnancy (see Adrenal gland symptoms) Ovarian tumour during pregnancy Luteoma of pregnancy Congenital adrenal hyperplasia Hermaphrodism Klinefelter's syndrome Turner's syndrome Mixed gonadal dysgenesis Leydig cell hypoplasia ...

A lack of breast development may be secondary to congenital absence of glandular tissue, a systemic disorder, radiation therapy, congenital adrenal hyperplasia, gonadal dysgenesis, ...

Gonadal Dysgenesis (XO) see Turner syndrome
Gorlin syndrome
Gorlin-Goltz syndrome see Gorlin syndrome
GOSHS see Goldberg Shprinzten syndrome
Gout see Arthritis (Adult)
Granulomatous disease see Chronic Granulomatous disorder ...

See also: Cancer, Symptom, Pregnancy, Uterus, Surgery