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Activating TRPV3 channels stops hair growth by killing hair follicle cells.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that PCOS in adolescents is complex and requires comprehensive care to manage its symptoms and associated health risks.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Woolly hair is a rare genetic condition with no effective treatments.

The document does not determine if adults with aphallia are fertile.

Stopping minoxidil caused significant hair loss, but regrowth occurred after resuming use.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Acne not improved by usual treatments may indicate a genetic disorder.

ECCL should be considered in patients with specific skin and eye lesions.

New genes and pathways are important for testosterone production and male sexual development.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Myoinositol helps improve menstrual cycles and some skin issues in women with PCOS.

Follistatin helps hair growth and cycling, while activin prevents it.

The report suggests that the same underlying issue in blood vessel support may cause angiokeratomas on both the scrotum and eyelids.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

A 13-year-old with 46 XY DSD had ambiguous genitalia due to incomplete masculinization.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.