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The document is a detailed guide on skin conditions and treatments for dermatologists.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

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

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

NF-κB is crucial for different stages and types of hair growth in mice.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

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

Edar signaling is crucial for controlling hair growth and regression.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

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

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

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found genes linked to hair loss in male giant pandas.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

The document concludes that understanding the sebaceous gland's development and function is key to addressing related skin diseases and aging effects.

Progress has been made in skin and nerve regeneration, but more research is needed to improve methods and ensure safety.

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

Light can turn on hair growth cells through a nerve path starting in the eyes.

Hair usually grows back 1-3 months after treatment for anagen effluvium, and children with Loose Anagen Hair Syndrome often improve by adolescence.

RANK-RANKL signaling is essential for hair growth and skin health.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.