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A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

New techniques can effectively treat aging around the eyes.

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

Hair transplants are effective for male and female pattern baldness, have evolved in technique, and require careful planning for natural results and managing complications.

Improve burn patients' appearance and function using various techniques, teamwork, and psychological support.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Understanding skin structure and development helps diagnose and treat skin disorders.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

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

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The study provides insights into hair growth mechanisms in yaks.

The document suggests using natural remedies like bloodletting and honey for various health issues but lacks scientific evidence for their effectiveness.

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

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

People with alopecia have a higher risk of thyroid cancer.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Satoyoshi syndrome is likely an autoimmune disease that mainly affects young women and improves with immune-related treatments.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

Diphenylcyclopropenone is more effective and has fewer side effects than dinitrochlorobenzene for treating alopecia areata.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document is a detailed medical reference on skin and genetic disorders.

The document concludes that diagnosing female hair loss requires careful examination, with treatments varying by condition and psychological support often necessary.