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Scalp biopsies from dermatomyositis patients show chronic hair loss without scarring, with mucin and blood vessel changes being very common.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

Researchers found a gene mutation responsible for a rare hair loss condition.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Cepharanthine may help hair growth by increasing IGF-I in scalp cells.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Breast implants are linked to autoimmune symptoms, with over half of patients feeling better after removal, but the exact cause is unclear and may involve bacterial biofilm.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

Lack of cystatin M/E causes thin hair and dry skin.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Doctors should use a detailed patient history and physical exam to diagnose joint pain, and consult a rheumatologist early for suspected autoimmune diseases.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Hair follicles and deer antlers regenerate similarly through stem cells and are influenced by hormones and growth factors.

The document concludes that accurate diagnosis is crucial for effectively treating various ear diseases in dogs and cats.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

The research suggests new treatments for skin cancer could target specific cell growth pathways.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Eosinophilia-myalgia syndrome, linked to contaminated L-tryptophan supplements, caused severe symptoms and some deaths, with long-term effects in survivors.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

Early treatment and weight management are important for teenagers with PCOS to reduce symptoms and long-term health risks.

The document says that common skin conditions in adult women can be treated effectively, with acne being the most common and early-detected melanoma having a high survival rate.

A 65-year-old woman has a growing bald spot on her scalp.

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