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A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

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

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

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

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

The document explains how to identify different hair problems using a microscope.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Acitretin helped improve hand mobility and skin condition in a patient.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

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

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.