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In the Jazan region of Saudi Arabia, hair loss is common, especially among women, older people, and those with higher education and BMI. Stress, poor nutrition, and hormonal changes are key causes, but many don't seek medical help.

Niosomes improve minoxidil skin delivery for hair loss treatment.

PCOD mainly affects young women, causing symptoms like irregular periods and weight gain, with mixed success from lifestyle changes and medication.

Homeopathic treatment can help manage alopecia areata in children.

Combining calcipotriol with mometasone is more effective for treating alopecia areata than using mometasone alone.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Herbal hair oil made with natural ingredients helps reduce hair loss, dandruff, and graying.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Premature graying of hair is common and stressful, but not well understood or treated.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Inositol shows promise in treating PCOS and other health issues, but more research is needed.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Nanomaterials show promise in improving wound healing but require more research on their potential toxicity.

Treating hair loss in both men and women is effective and improves quality of life.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Long-COVID has diverse, long-term health impacts, especially in young people.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Laser treatment effectively increases hair density and thickness in androgenic alopecia.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The document concludes that proper diagnosis and combined treatments are key for hirsutism management, and weight loss may help overweight patients.

Severe Hidradenitis Suppurativa increases missed and unproductive workdays.

Abrocitinib at 100 mg and 200 mg daily may significantly improve moderate-to-severe atopic dermatitis in patients 12 years and older.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

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