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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

Reflectance confocal microscopy is a useful, non-invasive tool for diagnosing some skin diseases, with potential for future improvements.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

New treatments for hair loss may target specific pathways and generate new hair follicles.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

FAI values above 6.4 may suggest high androgen levels and increased metabolic risks in Chinese women of reproductive age.

Human body's immune cells are more common in the layer of fat just beneath the skin than in deeper fat layers.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Mice with autoimmune hair loss showed signs of heart problems.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Abnormal cuticle and hair shaft medulla cause hair loss in androgenetic alopecia; sonography helps diagnose and manage it.

3D cell-derived matrices improve tissue regeneration and disease modeling.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

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

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Measuring the distance from the anus to the clitoris may moderately help diagnose polycystic ovary syndrome, especially in certain cases.

Researchers developed a new method to find substances in herbs that can block a specific enzyme linked to hair loss.

Melanoma development can be linked to the breakdown of skin's melanin-producing units.

AMH is a good marker for diagnosing PCOS, but global standards are needed.

Genomic approach finds new possible treatments for hair loss.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

Overexpressing SIMK in alfalfa boosts root hair growth, nodule clustering, and shoot biomass.

Medications for enlarged prostate can cause sexual side effects like reduced libido, erectile dysfunction, and ejaculatory problems.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

New technologies help us better understand how skin microbes affect skin diseases.