gonadal dysgenesis

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gonadal dysgenesis

[gō′nad·əl dis′jen·ə·səs]
(medicine)
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Most of the secondary sexual characteristics do not develop, and menses are absent in the majority of phenotypically female patients with pure gonadal dysgenesis.
Leukodystrophy in patients with ovarian dysgenesis.
Beyond 90 days, evaluate for PCOS, eating disorders, thyroid disease, hyperprolactinemia, gonadal dysgenesis, or premature ovarian failure.
Magnetic resonance imaging of the brain was normal, without evidence of dysgenesis.
THE ROLE OF PITX2 IN ANTERIOR SEGMENT DYSGENESIS IN HOUNTAIN HORSE BREEDS.
6% of the cases, hydronephrosis was caused by congenital dysgenesis of the ureteric muscular layer in the area of the pyeloureteral segment (PUS).
For example, in a matter of days, Puffenburger, et al, mapped sudden infant death with dysgenesis of the testes syndrome, or SIDDT, to a novel loss of function in the TSPYL gene using a 10K SNP genome array.
Dysembryogenesis, or dysgenesis, congenital hypothyroidism, which accounts for 85% of cases, results from ectopic thyroid tissue at the base of the tongue or in any position along the thyroglossal tract, agenesis, and hypoplasia.
The latter group of mice is particularly interesting due to hybrid dysgenesis resulting in undersize placentas and embryos.
But the disorder, named sudden infant death and dysgenesis of the testes syndrome (SIDDT) by researchers, might provide clues to the causes of other unexplained cases of cot death.
But the disorder, named sudden infant death and dysgenesis of the testes syndrome (SIDDT) by the researchers, might provide clues to the causes of other unexplained cases beside those within the Amish population.