Which Of The Following Is True Of Untreated Genetic Females With Adrenogenital Syndrome?

92 Which of the following is true of untreated genetic females with adrenogenital syndrome. B high levels of adrenal androgens. In females hypogonadism can cause sexual infantilism or abnormal pubertal development infertility and other reproductive system abnormalities. Adrenal crisis including hyponatremia and shock especially in newborns Abnormal female external genitalia internal organs are normal. Females may have a smaller opening of the vagina and lower fertility. Genetics edit CAH results from mutations of genes for enzymes mediating the biochemical steps of production of mineralocorticoids glucocorticoids or sex steroids from cholesterol by the adrenal glands steroidogenesis. Treatment with glucocorticoids leads quickly to feminization development of mammary glands the appearance of menstruation until the restoration of childbearing function.

Females may have a smaller opening of the vagina and lower fertility.

With congenital adrenogenital syndrome in persons with a genetic and gonadal female sex it is only expedient to choose a female gender. E none of the above. With congenital adrenogenital syndrome in persons with a genetic and gonadal female sex it is only expedient to choose a female gender. B the administration of cortisol. 81 Genetic males with androgenic insensitivity syndrome have. D increased interest in motherhood.

References In Congenital Adrenal Hyperplasia The Lancet

Which of the following is true of untreated genetic females with adrenogenital syndrome?. It can be questioned whether the low risk of virilized female newborns in untreated women with NCAH justifies prenatal diagnosis and treatment. Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency NCAH is a milder and later onset form of a genetic condition known as congenital adrenal hyperplasiaSome people affected by the condition have no associated signs and symptoms while others experience symptoms of androgen male hormone excessWomen with NCAH are generally born with normal female genitalia. At the birth of a child with an intersexual structure of the external genitalia and the absence of palpable testicles the study of sex chromatin should be an obligatory diagnostic method of research which makes it possible to avoid mistakes in determining the gender of congenital adrenogenital syndrome in girls.

D increased interest in motherhood. Males have normal fertility. Medication to treat this disorder must be continued for life.

Adrenal crisis including hyponatremia and shock especially in newborns Abnormal female external genitalia internal organs are normal. 85 If identified at birth in a genetic female adrenogenital syndrome is typically treated by early A surgical correction of any abnormalities of the genitals. 91 Adrenogenital teenage girls who have received neonatal cortisol therapy tend to display.

E early- onset dating. 86 Adrenogenital syndrome is associated with. Females may have a smaller opening of the vagina and lower fertility.

21-hydroxylase deficiency in the newborn and during infancy. 82 Which of the following is not a true statement about genetic males with androgenic insensitivity syndrome. Treatment with glucocorticoids leads quickly to feminization development of mammary glands the appearance of menstruation until the restoration of childbearing function.

O closing of the internal sphincter O opening of the external sphincter contraction of the seminal vesicles all of the above QUESTION 42 Male habitus physical appearance in a genetic female can result from. E all of the above. B They have ovaries.

B the administration of cortisol. A They have testes.

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C the administration of testosterone.

134 Three Cases of Exceptional Human Development. 86 Adrenogenital syndrome is associated with. In this disorder genetic males under most circumstances show sexual precocity whereas genetic females exposed to excessive amounts of androgens during early development may be born with. Medication to treat this disorder must be continued for life. A little public hair. 81 Genetic males with androgenic insensitivity syndrome have. E all of the above. In females hypogonadism can cause sexual infantilism or abnormal pubertal development infertility and other reproductive system abnormalities. 91 Adrenogenital teenage girls who have received neonatal cortisol therapy tend to display.

It can be questioned whether the low risk of virilized female newborns in untreated women with NCAH justifies prenatal diagnosis and treatment. With congenital adrenogenital syndrome in persons with a genetic and gonadal female sex it is only expedient to choose a female gender. Medication to treat this disorder must be continued for life. 85 If identified at birth in a genetic female adrenogenital syndrome is typically treated by early A surgical correction of any abnormalities of the genitals. A little public hair. In this disorder genetic males under most circumstances show sexual precocity whereas genetic females exposed to excessive amounts of androgens during early development may be born with. It can be questioned whether the low risk of virilized female newborns in untreated women with NCAH justifies prenatal diagnosis and treatment.