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Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The book "Hair Science and Technology" provides a deep understanding of hair biology and genetics, discusses hair growth, density, and diseases, and offers methods for managing hair loss and caring for hair growth.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The document concluded that FDA-approved treatments like minoxidil and finasteride are effective for hair loss, while the effectiveness of natural remedies and other non-approved treatments is not well-supported by evidence.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Biomaterials with MSC-derived substances could improve tissue repair and have advantages over direct cell therapy.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

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.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

New genetic discoveries may lead to better treatments for alopecia areata.

Keratins are important for skin cell health and their problems can cause diseases.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.