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Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Polycystic ovary syndrome affects about 6-10% of women, with varying symptoms and the need for standardized global definitions.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Men with early hair loss have similar hormone levels to women with PCOS, possibly increasing risk of obesity and heart issues.

Growth media with sucrose and gelrite significantly enhance Arabidopsis root hair growth.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Premature hair graying in the face may be influenced by genetics and environment.

The study found that PCOS affects about 6.5-6.8% of women in both urban and rural areas of Telangana, India, and highlighted the importance of lifestyle changes for management.

Using a blow dryer in a certain way can cause localized hair damage with bubble formation inside the hair.

Conditioned media from mesenchymal stem cells show promise for tissue repair and disease treatment, but more research is needed on their safety and effectiveness.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Melatonin improves cashmere goat hair growth and quality by increasing antioxidants and reducing cell death.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

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

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Most people with basal cell carcinoma on their head or neck were 60-70 years old, and it often came back even after being fully removed, especially in certain areas and types.

Women with Polycystic Ovary Syndrome (PCOS) have a lower health-related quality of life, especially those with an anovulatory phenotype, and may need specific interventions to improve it.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Studying rare genetic disorders can help us understand and treat common diseases better.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Oestrogens are key for bone growth during puberty in both boys and girls.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.