dysgenesis मीनिंग इन हिंदी

अधिक: आगे

In contrast XX gonadal dysgenesis has a normal female chromosome situation.
Congenital hypothyroidism caused by thyroid dysgenesis can be associated with PAX8.
The P element gives rise to a phenotype known as hybrid dysgenesis.
Women with 46 XX gonadal dysgenesis experience primary amenorrhea with hypergonadotropic hypogonadism.
Mutations in the FOXE3 gene are associated with anterior segment mesenchymal dysgenesis.
The term dysgenesis is used to describe abnormal organ development during embryonic growth and development.
Although similar in some ways to mixed gonadal dysgenesis, the conditions can be distinguished histologically.
Microcornea and iridocorneal dysgenesis also occur.
In the rabbit model, disorders observed involving NR4A1 expression include testicular dysgenesis, and cryptorchidism.
Other disorders that result from STRA6 mutations include pulmonary dysgenesis, cardiac malformations, and mental retardation.

संज्ञा.