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Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

CD2 might be a new treatment target for patchy alopecia areata.

Tattooing helps treat skin conditions, reconstruct nipple-areola, mark radiation fields, and locate lesions.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

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

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Hair and wool have diverse keratins and keratin-associated proteins.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Assessing newborn scalp hair can reveal important health information.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

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

The document concludes that while significant progress has been made in understanding skin biology and stem cells, more research is needed to fully understand their interactions with their environment.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Twins had rare skin cysts likely due to genetics.