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  2. Human penis - Wikipedia

    en.wikipedia.org/wiki/Human_penis

    Phimosis is an inability to retract the foreskin fully. It is normal and harmless in infancy and pre-pubescence, occurring in about 8% of boys at age 10. According to the British Medical Association, treatment (topical steroid cream and/or manual stretching) does not need to be considered until age 19.

  3. Topical glucocorticoids - Wikipedia

    en.wikipedia.org/wiki/Topical_glucocorticoids

    Placement of occlusive dressing on the body area, that will raise the absorption rate [11] The differences in extent of percutaneous absorption in different parts of the body (percent of the total dose absorbed into the body through the skin) are as follows: [9] Sole – 0.05%; Palm – 0.1%; Forearm – 1%; Scalp – 3.5%; Face – 7%

  4. How to get rid of body odor, according to medical experts - AOL

    www.aol.com/rid-body-odor-according-medical...

    Some of the best ways to combat body odor, per experts, include: Regular bathing, which removes bacteria from the skin, per Harvard Health. Some people may only need to shower or take a bath a few ...

  5. Phimosis - Wikipedia

    en.wikipedia.org/wiki/Phimosis

    Physiologic phimosis, common in males 10 years of age and younger, is normal, and does not require intervention. [26] [35] [27] Non-retractile foreskin usually becomes retractable during the course of puberty. [27] If phimosis in older boys or adult males is not causing acute and severe problems, nonsurgical measures may be effective.

  6. Prednisolone - Wikipedia

    en.wikipedia.org/wiki/Prednisolone

    Prednisolone is a synthetic pregnane corticosteroid closely related to its cognate prednisone, having identical structure save for two fewer hydrogens near C 11. It is also known as δ 1-cortisol, δ 1-hydrocortisone, 1,2-dehydrocortisol, or 1,2-dehydrohydrocortisone, as well as 11β,17α,21-trihydroxypregna-1,4-diene-3,20-dione. [50] [51]

  7. List of corticosteroids - Wikipedia

    en.wikipedia.org/wiki/List_of_corticosteroids

    Most esters of these corticosteroids are not included in this list; for esters, see here instead. The most common structural modifications in synthetic corticosteroids include 1(2)- dehydrogenation , 6α-, 9α-, 16α-, and 16β- substitution (with a halogen or methyl group ), 16α,17α- acetonidation , and 17α- and 21- esterification .