congenital adrenal hyperplasia การใช้

• It is a marker of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
• Addison's disease and congenital adrenal hyperplasia can manifest as adrenal insufficiency.
• Skinner's PhD involved developing genetic tests to detect congenital adrenal hyperplasia in children.
• POR deficiency is the newest form of congenital adrenal hyperplasia first described in 2004.
• This, however, only applies to cases involving congenital adrenal hyperplasia and other intersex situations.
• Girls who have congenital adrenal hyperplasia ( CAH ) typically engage in more rough-and-tumble play.
• Girls with congenital adrenal hyperplasia ( CAH ) have atypically high blood concentrations of testosterone.
• Women with congenital adrenal hyperplasia reported more male-typical play behaviours and showed less heterosexual interest.
• Rarer causes include precocious puberty, congenital adrenal hyperplasia, and androgen-producing tumors of the adrenals or gonads.
• It can be used in congenital adrenal hyperplasia in older adolescents and adults to suppress ACTH production.
• Hormonal disorders such as congenital adrenal hyperplasia ( CAH ) offer clues about the role of hormones.
• Other examples include complete androgen insensitivity syndrome, partial X chromosome deletions, lipoid congenital adrenal hyperplasia, and Turner syndrome.
• Doctors who ran tests diagnosed congenital adrenal hyperplasia, a condition that, put simply, can make baby girls'genitals look male.
• See congenital adrenal hyperplasia for a more detailed discussion of androgen suppression and fertility potential in adolescent and adult women.
• Part 3 interviews parents of children with complete androgen insensitivity syndrome and congenital adrenal hyperplasia, and adults with intersex experiences.
• _Congenital adrenal hyperplasia, an inherited disorder affecting one baby in 5, 000, involving defects in the synthesis of adrenal hormones.
• Of the synthesis problems, congenital adrenal hyperplasia is the most common ( in various forms : StAR and mitochondrial DNA mutations.
• V鰈ling was born in 1959 with XX sex chromosomes, typically associated with being female, and likely also with congenital adrenal hyperplasia.
• Nonstop mutations have been linked with several congenital diseases including congenital adrenal hyperplasia, variable anterior segment dysgenesis, and mitochondrial neurogastrointestinal encephalomyopathy.
• The latter applies in particular to Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, which is the most common form of CAH.