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Some people with pattern hair loss may also have scalp inflammation and scarring similar to lichen planopilaris.

Omeprazole effectively treats severe acid reflux in children for short-term use, but long-term safety needs more research.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Lupus affects the body and skin, causing joint pain and skin issues that can be treated with steroids and antimalarial drugs.

Skin aging is due to impaired stem cell mobilization or fewer responsive stem cells.

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.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

The conclusion is that FFA and LPP have similar scalp biopsy features, making them hard to distinguish histologically, and FFA may be a specific kind of scarring hair loss.

Applying a special compound can promote hair growth without harmful side effects.

Oral retinoids are effective for various skin conditions but have side effects and should not be used during pregnancy.

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.

Alpha-hydroxy acids, like glycolic acid, safely improve skin issues and work on all skin types.

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

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.

Papain and bisulfite break down human hair by dissolving parts of it.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

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

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Most low-level light therapy studies did not accurately report how light was measured, affecting treatment reliability.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

PEGL-DOX causes Hand-Foot Syndrome due to skin reactions from prolonged circulation and ROS generation.

Docetaxel and paclitaxel for breast cancer can cause permanent, severe hair loss.