Search

everythinglearnresearchcommunity

for

Search:↓

Minoxidil stimulates hair growth by increasing hair thickness and prolonging growth phase.

Some skin medications can harm male fertility, but they don't seem to cause birth defects from father's exposure.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Ethinylestradiol/chlormadinone acetate may be an effective and well-tolerated treatment for skin conditions caused by excess androgens.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

New treatments for a chronic skin condition show promise, but individualized plans are crucial due to varying responses.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The Endocrine Society advised against routine testosterone therapy for women, citing a need for more research on long-term safety and a clear definition of androgen deficiency.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Postmenopausal hyperandrogenism, a condition with symptoms like increased hair growth and acne, is usually caused by PCOS but can also be due to other factors. It's diagnosed by checking testosterone levels and treated either by removing the adrenal tumor or through antiandrogen therapy.

A specific gene mutation causes congenital hair loss.

Hair analysis can help diagnose adrenal disorders non-invasively.

Gene mutations can cause problems in male genital development.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

Researchers found a new mutation causing total hair loss from birth.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Hormone imbalances from the pituitary, thyroid, and adrenal glands can cause infertility, but treating these disorders can improve fertility.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Minoxidil is effective for hair growth and safe for long-term use.

The study concluded that neonatal occipital alopecia is common, not caused by physical friction, and usually resolves on its own without treatment.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The document concludes that research on sulfatase inhibitors should continue due to their potential in treating various diseases, despite some clinical trial failures.

The conclusion is that published guidelines are improving transgender medical care, but more research and education in transgender medicine are needed.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

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