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Tinea capitis, a scalp fungal infection in children, is best treated with newer antifungal agents for shorter periods.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Two patients with porphyria cutanea tarda experienced their grey hair turning dark again.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Hair relaxers are linked to reduced cystine levels and potential hair damage.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Combining systemic and topical treatments, guided by weekly fungal cultures, effectively treats cat ringworm.

Healthy dogs and cats can carry and spread skin infections without showing symptoms.

Toxic Shock Syndrome progresses quickly, often involves multiple organs, and is linked to Staphylococcus aureus toxins, with treatment options available but diagnostic challenges remaining.

Birth control pills increase the risk of blood clots, especially within the first year and with certain types.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

A man's rare tumor caused unusual nerve-related symptoms that improved after surgery.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

New treatments for children's scalp ringworm are recommended based on recent data.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Canadian porcupines in a Japanese zoo passed a skin fungus to each other.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Woman's hair loss diagnosis changed from CTE to AA; multiple biopsies important for accurate diagnosis.