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Pili anulati may cause hair loss, proper diagnosis and treatment needed.

Hair loss in women is often due to hereditary conditions or stress, and while treatments like minoxidil can help, diagnosis and management require medical guidance.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

An adult with Kawasaki disease experienced temporary heart failure but recovered without lasting heart damage.

Some skin diseases and anaemia are related, and treating the skin condition can often improve the anaemia.

Rac1 is essential for proper hair structure and color.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Targeted cancer therapies often cause skin problems that need careful management to improve patient quality of life and treatment success.

Vitamin A toxicity can cause severe health issues and may require a liver transplant if other treatments fail.

Every elderly patient had at least one skin condition, often linked to other diseases, highlighting the need for integrated skin and general healthcare in the elderly.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Dermoscopy and trichoscopy are useful for diagnosing skin signs in Dermatomyositis.

Retinol acetate can reduce the harmful effects of the drug benoxaprofen on white blood cells.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Hair growth and development are controlled by specific signaling pathways.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

About 12% of children in Kota, Rajasthan, experience hair loss, mainly due to fungal infections, with early treatment advised to prevent worsening.

Tofacitinib is effective and has minor, reversible side effects for treating severe hair loss in Iran.

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.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.