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Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Topical botanical lotion increases hair density and improves quality of life in women with hair loss.

The Itpr3 gene causes a specific hair pattern in mice.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

Updated treatments for female hair loss include minoxidil, antiandrogens, hair transplants, and light therapy.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

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

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Review finds no permanent solution for female hair loss.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Turkish herbal cosmetics use various plants for hair care, skincare, and other personal hygiene purposes.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Finasteride can have lasting negative effects on brain function and behavior by disrupting neurosteroid production.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.