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Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Children need early diagnosis and treatment for iron-deficiency anemia to prevent learning problems and promote health.

The guide explains how to diagnose and treat hair loss in dogs, covering causes and treatments, with some conditions lacking treatment options.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hair disease research is a growing and evolving field in dermatology, with recent significant advances.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

The conclusion is that certain cell interactions and signals are crucial for hair growth and regeneration.

The study found that sweat glands contain different types of stem cells that help with healing and maintaining healthy skin.

Growing human skin cells in a 3D environment can stimulate new hair growth.

Lactate production is important for activating hair growth stem cells.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Stem cell plasticity is crucial for wound healing but can also contribute to cancer development.

Stress increases nerve fibers and immune cell activity in mouse skin, possibly worsening skin conditions.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Fetal skin heals without scarring due to unique cells and processes not present in adult skin healing.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Stress from being transgender is linked to higher blood pressure at night and more inflammation, which may affect heart health.

Spiny mice are better at regenerating hair after injury than laboratory mice and could help us understand how to improve human skin repair.