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Hypothyroidism patients with hair loss typically have thinning hair, smaller hair follicles, and normal hair shedding.

Scientists created a new cell line from Cashmere goat hair and found that cytokeratin 13 is a unique marker for certain skin cells.

The most effective way to diagnose non-scarring hair loss is by transverse sectioning, and some cases, particularly in males with inflammation around hair follicles, might be curable.

The conclusion is that a new method could improve the identification of autoimmune targets in alopecia areata, despite some limitations.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

Dermoscopy helps diagnose different scalp conditions by showing unique signs for each disorder.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Melanocytes from human fetal hair follicles were successfully cultured, showing potential for hair disease research and clinical use.

Oral zinc sulphate is an effective and safe treatment for thallium poisoning, especially for skin and hair symptoms.

Hair transplants for male baldness can show inflammation and fibrosis, but more research is needed to confirm LPP presence.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

The woman's skin and hair symptoms were confirmed as frontal fibrosing alopecia, and while facial papules are common in such cases, there's no effective local treatment, but systemic treatments can help.

Skin problems like psoriasis and systemic sclerosis can increase the risk of heart disease, so doctors should watch for heart risks in patients with these conditions.

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

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

Early detection and treatment of folliculitis keloidalis can prevent disease progression.

Primary care should recognize and treat hair loss in hijab-wearing individuals with cultural sensitivity.

Many hospitalized children with COVID-19 had skin, mouth, or nail changes, with skin rashes being common.

Low-dose oral minoxidil can cause serious heart complications.

The nervous system helps control stem cell behavior and immune responses, affecting tissue repair and maintenance.

Trichoscopy is a valuable, quick, and non-invasive tool for diagnosing tinea capitis in children.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Understanding the genetics of alopecia areata could lead to better treatments.

Krox20 overexpression in fibroblasts may play a role in abnormal scar formation and could be a target for new treatments.

Lupus erythematosus can mimic alopecia areata, and trichoscopy is key for accurate diagnosis and better patient outcomes.

Alopecia areata shows various signs on the skin that aid in diagnosis and prognosis, with certain features indicating more severe disease.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.