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Some Middle Eastern plants may help treat diabetes and could be alternatives to current drugs, but more research is needed.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

New hair transplant methods offer more natural results and better graft survival, with ongoing research to increase donor hair options.

Hypaphorine from a fungus changes the internal structure of Eucalyptus root hairs, stopping their growth.

Telogen effluvium is a hair loss condition with acute cases resolving quickly and chronic cases potentially lasting longer, sometimes requiring treatment.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Hair loss in women not always linked to increased oil production; other factors may be involved.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Ultrasound shows 80% of Hidradenitis Suppurativa patients have abnormal hair tracts that may worsen the condition.

Thyroid hormones are important for skin health and might help treat skin diseases, but more research is needed to understand their effects fully.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Hair loss in elderly women is often caused by various factors, including hormonal changes after menopause.

Higher aldosterone levels link to hair loss and high blood pressure.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Small changes in hormones can significantly impact health, showing the importance of sensitive testing for chemicals that disrupt hormones.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Sensitive skin often causes discomfort, affects many people, especially women and older adults, and should be managed with careful product selection.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Minoxidil use during pregnancy may cause fetal harm.

Higher minoxidil doses in dogs cause faster heart rate, lower blood pressure, and heart issues.

Women with PCOS have higher levels of AMH in their blood and follicles, and this can help predict their risk of overreaction to fertility treatments.

Hair transplantation may work for some types of scarring alopecia, but results vary and more research is needed.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.