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Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Innovative methods are reducing animal testing and improving biomedical research.

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

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

The document concludes that sex hormones and related compounds have various effects on health, with both potential benefits and risks.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

A new vaccine using a porous scaffold boosts immunity and protects against the flu better than traditional methods.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Oral contraceptives provide various health benefits beyond birth control, including managing menstrual issues, skin conditions, pain, and reducing the risk of certain cancers.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

New genetic mutations linked to rare skin disorders were found in three newborns.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

Finasteride-loaded nanogels are effective, safe, and improve drug absorption through the skin.

People with Type 2 Diabetes are more likely to have a mite infestation called Demodex folliculorum.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Combination pharmacotherapy is generally more effective for treating keloids and hypertrophic scars.

Finasteride may lower cholesterol and slow heart disease progression.

COVID-19 may harm male reproductive health and lower testosterone levels, potentially affecting fertility and causing erectile dysfunction. More research is needed.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

PCOS treatment should address both symptoms and metabolic risks, starting with lifestyle changes and possibly including medication.

Hormone treatment for transsexual individuals is effective but carries risks like thromboembolic events and mood changes, with most side effects being minor and reversible.

Menopause significantly reduces skin collagen, leading to thinner, less elastic skin, and hormone replacement may help but requires careful consideration.

Antiandrogens can help treat skin conditions like acne and excessive hair in women when used carefully.