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The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

The patient was diagnosed with celiac disease after a long delay, showing the need for better awareness and earlier detection.

The document concludes that hair loss in women is complex, often linked to aging, health conditions, and nutritional deficiencies, and emotional impacts should not be underestimated.

An 18-year-old girl improved with treatment after being diagnosed with both Systemic Lupus Erythematosus and Celiac Disease.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Hair regrowth slows with age and can be affected by treatments that change enzyme activity in the skin.

Minoxidil sulfotransferase is a marker of keratinocyte differentiation and may play a role in hair growth.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Celiac disease can cause skin problems that may get better with a gluten-free diet.

PDI helps restore over-bleached hair's strength and structure by attaching special peptides.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Researchers created a skin treatment that could effectively deliver medication into hair follicles.

Thyroid hormones affect skin texture, hair and nail growth, and can cause skin diseases related to thyroid problems.

Scalp pain is a common symptom in people with active hair loss from telogen effluvium.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

Vitamin B12 deficiency can cause skin darkening and increased blood vessels, but treatment can improve symptoms.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A gluten-free diet stopped a child's hair-eating behavior and suggested she had celiac disease.

Involucrin helps strengthen the inner parts of human hair.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

Higher antigliadin antibody levels are linked to alopecia areata severity.

Collagen XVII is crucial for skin cell growth and nail health.

Adult skin cells can be used to create new hair in a lab.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.