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Specific and forms
Specific poetic forms have been developed by many cultures.
Specific forms of theft and other related offences
Specific integers known to be far larger than Graham's number have since appeared in many serious mathematical proofs ( e. g., in connection with Friedman's various finite forms of Kruskal's theorem ).
Specific forms of vaginitis are:
Specific forms of art were developed in Georgia for religious purposes.
Specific deadlines, procedures, and forms may be required.
Specific absorption rate ( SAR ) is a measure of the rate at which energy is absorbed by the body when exposed to a radio frequency ( RF ) electromagnetic field ; although, it can also refer to absorption of other forms of energy by tissue, including ultrasound.
Specific forms of the grip are French grip, German grip, and American grip.
Specific forms of payment systems are also used to settle financial transactions for products in the equity markets, bond markets, currency markets, futures markets, derivatives markets, options markets and for transfer funds between financial institutions both domestically using clearing and Real Time Gross Settlement ( RTGS ) systems and internationally using the SWIFT network.
Specific master wood carvers also subtly modified the accepted ( or even religiously mandated ) local forms, forming a distinct " signature " or " school " of Chiwara figures.

Specific and adrenal
Specific to the activation of the hypothalamo-pituitary adrenal axis, norepinephrine will stimulate the secretion of corticotropin-releasing factor from the hypothalamus, which induces adrenocorticotropic hormone release from the anterior pituitary and subsequent cortisol synthesis in the adrenal glands.

forms and congenital
All of the congenital metabolic defects, congenital forms of hyperinsulinism, and congenital hypopituitarism are likely to have already been diagnosed or are unlikely to start causing new hypoglycemia at this age.
Some forms of congenital hyperinsulinism respond to diazoxide or octreotide.
Generally, there are two forms of syringomyelia: congenital and acquired.
Other forms of diabetes mellitus include congenital diabetes, which is due to genetic defects of insulin secretion, cystic fibrosis-related diabetes, steroid diabetes induced by high doses of glucocorticoids, and several forms of monogenic diabetes.
Both genetic ( e. g., Berardinelli-Seip congenital lipodystrophy, Dunnigan familial partial lipodystrophy ) and acquired ( e. g., HIV-related lipodystrophy in patients treated with highly active antiretroviral therapy ) forms of lipodystrophy may give rise to severe insulin resistance and many of metabolic syndrome's components.
Cuba declared the disease eliminated in the 1990s, and in 2004 the Centers for Disease Control and Prevention announced that both the congenital and acquired forms of rubella had been eliminated from the United States.
Both forms can be either congenital or acquired.
There is no ideal therapy for neutropenia, but recombinant G-CSF ( granulocyte-colony stimulating factor ) such as filgrastim can be effective in chemotherapy patients, in patients with congenital forms of neutropenia including severe congenital neutropenia, autosomal recessive Kostmann's syndrome, cyclic neutropenia, and myelokathexis.
# Certain forms of congenital adrenal hyperplasia
The congenital forms of the disorder are considered stationary and do not worsen with age.
The known causes of the congenital forms of achromatopsia are all due to malfunction of the retinal phototransduction pathway.
Septo-optic dysplasia is one of the most common forms of congenital growth hormone deficiency.
Many disorders of immune system function can affect the formation of active immunity such as immunodeficiency ( both acquired and congenital forms ) and immunosuppression.
The autosomal recessive forms of LQTS tend to have a more severe phenotype, with some variants having associated syndactyly ( LQT8 ) or congenital neural deafness ( LQT1 ).
The reported cases suggest that this form of the disorder may be heritable and much more common than previously thought ( about 2. 5 % of the population may be affected ), although this congenital disorder is commonly accompanied by other forms of visual agnosia, and may not be " pure " prosopagnosia.
Medical diagnosis of the two forms of congenital dextrocardia can be made by ECG or imaging.
Biliary atresia, also known as " extrahepatic ductopenia " and " progressive obliterative cholangiopathy " is a congenital or acquired disease of the liver and one of the principal forms of chronic rejection of a transplanted liver allograft.
Examples of undervirilization are androgen insensitivity syndrome, 5 alpha reductase deficiency, and some forms of congenital adrenal hyperplasia.
Management of salt-wasting crises and mineralocorticoid treatment are as for other forms of salt-wasting congenital adrenal hyperplasias: saline and fludrocortisone.
** Some forms of congenital adrenal hyperplasia

forms and adrenal
The other forms of ALD vary in terms of onset and clinical severity, ranging from adrenal insufficiency to progressive paraparesis in early adulthood ( this form of the disease is typically known as adrenomyeloneuropathy ).
Synthetic glucocorticoids are used in the treatment of joint pain or inflammation ( arthritis ), temporal arteritis, dermatitis, allergic reactions, asthma, hepatitis, systemic lupus erythematosus, inflammatory bowel disease ( ulcerative colitis and Crohn's disease ), sarcoidosis and for glucocorticoid replacement in Addison's disease or other forms of adrenal insufficiency.
Despite this distinction, Addisonian crises can happen in all forms of adrenal insufficiency.
As with other forms of adrenal insufficiency, extra glucocorticoid is needed for stress coverage.
As with other forms of CAH, the primary therapy of 11β-hydroxylase deficient CAH is lifelong glucocorticoid replacement in sufficient doses to prevent adrenal insufficiency and suppress excess mineralocorticoid and androgen production.
Milder forms resulting from incomplete loss of 3β-HSD type II function do not present with adrenal crisis, but can still produce virilization of genetically female infants and undervirilization of genetically male infants.
Like other forms of CAH, 17α-hydroxylase deficiency impairs the efficiency of cortisol synthesis, resulting in high levels of ACTH secretion and hyperplasia of the adrenal glands.
This surgery is performed on women with androgen insensitivity syndrome, congenital adrenal hyperplasia, vaginal agenesis, müllerian agenesis, and other intersexual conditions wherein non-invasive forms of deepening the vagina cannot be performed ( mostly on trans women patients ) as an alternative to penile inversion, with or without an accompanying skin graft ( usually from the thigh or the abdomen ).
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency ( 21-OH CAH ), in all its forms, accounts for over 95 % of diagnosed cases of congenital adrenal hyperplasia, and " CAH " in most contexts refers to 21-hydroxylase deficiency.
The specialty also deals with hypoglycemia and other forms of hyperglycemia in childhood, variations of puberty, as well other adrenal, thyroid, and pituitary problems.

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