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A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

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

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Assessing newborn scalp hair can reveal important health information.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

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

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

No link found between new male baldness genes and female hair loss.

Detailed patient history and physical exams are crucial for diagnosing hair loss.

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 mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

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

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Psychotropic drugs can cause hair loss or excessive hair growth.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.