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Anti-IL-12/IL-23 antibody therapy effectively treats psoriasiform skin lesions in IBD patients.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

Male pattern baldness involves genetics, hormones, and needs better treatments.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

The niche environment controls stem cell behavior and plasticity, which is important for tissue health and repair.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

Understanding how cells die in the skin is important for treating skin diseases and preventing hair loss.

Some drugs can cause skin, nail, and hair problems, which are important for healthcare professionals to recognize and report.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

EDA2R gene linked to hair loss.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

Scientists found a gene in mice that causes early hearing loss.

Immunosuppressive and anti-TNF therapies in IBD patients can increase the risk of skin cancer and cause various skin issues.

People with polycystic ovary syndrome have a higher chance of having chronic thyroiditis.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Two-photon microscopy helps observe hair follicle stem cell behaviors in mice.

DHT, a testosterone byproduct, causes male pattern baldness.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Blocking JAK/STAT pathways can help treat hair loss from alopecia areata.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

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

Early recognition and management of skin side effects from new cancer therapies can prevent treatment delays.