How to treat congenital adrenal hyperplasia quickly?

?Quickly? The diagnosis implys a genetic abnormality that will last a lifetime.It can be managed over time with the aid of metabolic disease specialists working in conjunction with your local source of health care. Daily medication & scheduled followup tests and exams will gauge the progress.

Related Questions

How to treat non-classical congenital adrenal hyperplasia?

Male or Female? This would depend on the age and sex of the patient in addition to the degree of severity. If cortisol response is normal and a male is affected, often times steroid suppression is stopped after puberty. This is more complicated in females who may otherwise suffer from irregular periods, hirsutism, recalcitrant acne. They may need treatment through adulthood. Please discuss with endocrinologist. Read more...

Who has congenital adrenal hyperplasia?

Enzyme deficiency. Deficiency of 21 hydroxylase enzyme needed for synthesis of gluco- and mineralo-corticoids causes excessive production of sex hormones, mainly male sex hormones. The result is endocrine disturbance in both boys and girls and virilization in girls. Read more...

What is congenital adrenal hyperplasia?

Enzyme defeciency. This disease results from deficiency of an enzyme, 21 hydroxylase, that is essential for synthesis of adrenal hormones. Block in the synthesis of glucoroticoids causes excess production of male sex hormones. See this site for more information. http://www.ncbi.nlm.nih.gov/pubmedhealth/pmh0001448/. Read more...

How long should congenital adrenal hyperplasia last?

Forever. This is a lifelong genetic issue. Medication & monitoring can decrease the impact on one's life, but it is not like a pneumonia, it doesn't go away after treatment. Read more...

What are the tests for congenital adrenal hyperplasia?

ADRENAL HYPERPLASIA. Serum levels of 17-hydroxy progesterone, cortisol, corticosterone, Progesterone are low and dhea, androstenedione are high. Read more...
CAH testing . State newborn screening measures 17-oh progesterone. If elevated, this could mean cah in the newborn. 21 hydroxylase deficiency causing elevation in 17- ohp is the most common cause of cah. With infants this is usually associated with salt wasting. Aldosterone & cortisol are low. Acth will be high given low cortisol. Girls usually have ambiguous genitalia. Peds endo cares for kids w/cah. Read more...

What sort of disease is congenital adrenal hyperplasia?

Gene Mutation. A mutated form of the enzyme blocks the normal production of adrenal hormoes and causes excess production of male sex hormones on both male and female fetuses and babies. Read more...
Gene mutation. A mutated form of the enzyme blocks the normal production of adrenal hormoes and causes excess production of male sex hormones on both male and female fetuses and babies. Read more...
Missing enzyme. There are different types. They all involve a deficiency of an enzyme needed in cortisol production. Since the pituitary senses there isn't enough cortisol, it keeps trying to make the adrenals make cortisol. But because that enzyme is missing, the building blocks of cortisol build up. These substances get turned into androgens - male hormones - and cause abnormalities in sexual development. Read more...

What are the symptoms of congenital adrenal hyperplasia?

CUSHING's SYNDROME. Sx are moonface, truncal obesity, buffalo hump, slender extremities and fingers, striae of the abdomen, easy bruising and menstrual disorder secondary to elevated corticosteroids. Read more...
Classic or non? Classic cah is diagnosed mostly on newborn screening. It results from a block in the synthesis of cortisol and usually also aldosterone. Females will often have ambiguous genitalia. Males don't look different. Permanent replacement with Hydrocortisone & Fludrocortisone (may not need past childhood) are needed for sustaining life and salt balance. Pediatric endocrinologists follow very closely. Read more...

Do the symptoms of congenital adrenal hyperplasia differ by gender?

Yes. Persons with the most common form congenital adrenal hyperplasia (cah) have a predisposition to making extra testosterone. For girls this can manifest as genitalia that is "masculinized" before birth and therefore "ambiguous" at the time of birth. Girls can also have somewhat masculinized behaviors. The testosterone levels can be lowered by therapy. Boys do not have genital or behavioral issues. Read more...

What symptoms does someone with congenital adrenal hyperplasia have?

CAH. This is due to the lack of an enzyme needed for the adrenals to make cortisol and aldosterone. The body then uses the precursors to make androgen (male hormones) instead. Symptoms for girls: deep voice, abnormal menstruation, early appearance of pubic/armpit hairs, genitials looking both male and female...For boys: deep voice, enlarged penis, small testes, early appearance of pubic, armpit hair... Read more...
CAH symptoms. In females, it depends on whether it's classical or not. In classicals there is more severe early onset salt wasting and genital ambiguity. Much more common late onset non-classicals with lesser adrenal enzyme deficiencies have excessive hair growth, virilization, oligomenorrhea, and/or inferlility. Read more...