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A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Videodermoscopy is effective for diagnosing different types of non-scarring hair loss.

Clomipramine may significantly reduce hair-pulling in Trichotillomania, but more research is needed on treatments and early onset cases.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Certain bacteria from the Citrullus colocynthis plant may be a new source of antibiotics to fight drug-resistant diseases.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Hair's internal fibers are arranged in a pattern that doesn't let much water in, and treatments like oils and heat change how much water hair can absorb.

FUE hair transplants offer minimal scarring and are good for short hairstyles but are time-consuming and can be costly.

Eating disorders can cause various hair problems, and while hair loss in these disorders is linked to metabolic syndrome, treatment focuses on specific medications and lifestyle changes for the syndrome.

Keratin structure in hair is stable at pH 5-6 but disrupts between pH 6-7.

Hair transplant surgery is a good cosmetic solution for people with little or no pubic hair, especially to boost their self-esteem.

Researchers found a gene mutation responsible for a rare hair loss condition.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

New nanofiber technology improves wound healing by supporting cell growth and delivering treatments directly to the wound.

Using a scalp flap for hair transplantation gives denser, faster results than older methods, but it's complex and needs careful planning.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

A thorough history and examination are crucial for diagnosing skin diseases, which affect up to a third of people. This includes details about skin lesions, medication, general health, lifestyle, family, and contacts, as well as examining the rash, hair, nails, and mucous membranes. Changes in hair and nails can also indicate other medical and skin disorders.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Curved human hair has different structures on each side, which might cause its shape and is similar to wool.

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

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Some people's hair loss is caused by multiple factors, with the most common being a mix of AGA and CCCA.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Eclipta alba extract helps increase hair growth and decrease hair loss-related protein in mice.