Search

everythinglearnresearchcommunity

for

Search:↓

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Troglitazone increases subcutaneous fat in lipodystrophy patients.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Combining Traditional Chinese Medicine and Western medicine can improve symptoms, hormone levels, and pregnancy outcomes in Polycystic Ovary Syndrome patients, but more research is needed.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

The review provided information on various treatments to stop hair thinning and increase hair density in people with common genetic hair loss.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Male pattern baldness is a genetic condition causing hair loss, with limited but improving treatment options.

Doctors should prescribe Minoxidil, Finasteride, and Dutasteride for treating androgenetic alopecia.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Azathioprine caused side effects in over half of the Korean pediatric inflammatory bowel disease patients, requiring close monitoring.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Plant extracts may help treat hormone-related hair loss.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Androgenetic alopecia, a genetic disorder affecting up to 50% of adults, is caused by an excessive response to androgens leading to hair follicle shrinkage. Treatments include FDA-approved drugs, other therapies like low-dose oral minoxidil, and hair transplantation.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Hair loss can be treated based on its type and cause, improving quality of life.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Antioxidants and growth factors may help treat hair loss when combined with LED and Laser therapy.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Mesenchymal stromal cells may help treat severe COVID-19, but more research is needed to confirm their effectiveness.