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The conclusion is that in the Indian subcontinent, socioeconomic status, stress, and family structure affect the severity of alopecia areata, and its psychological impact is generally mild or moderate.

Alfatradiol (0.025%) is an effective and safe treatment for hair loss in both women and men.

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

Fractional laser treatment helped hair regrowth in patients with alopecia areata.

Hedgehog pathway inhibitors used for skin cancer can cause significant hair loss, which may improve after stopping the medication.

MC4R gene variants not linked to female hair loss.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Timolol eye-drops can cause hair loss.

Most spinal cord injury patients in Korea experience skin problems, especially fungal infections and eczema, affecting their quality of life.

Human hair follicles may provide a noninvasive way to diagnose diseases and have potential in regenerative medicine.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

New targeted cancer drugs can cause skin side effects, and managing them requires patient education and timely care.

People who get alopecia areata after age 50 usually have mild symptoms, high chances of hair regrowth, and often have other health conditions.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

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

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

The U.S. FDA regulates cosmetics for appearance purposes, but not as strictly as some other countries.

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

Using special RNA to target a mutant gene fixed hair problems in mice.

Most people with hypothyroidism have skin problems like dry skin and hair loss.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

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.

Treating both the mind and skin together, especially by managing stress, can greatly improve outcomes for skin disorders linked to psychological issues.

Changing hairstyles can help hair regrow in children with hair loss from tight braids or ponytails.

Alopecia areata can sometimes appear as a straight line of hair loss instead of round patches.