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SLHA can be hard to diagnose and needs teamwork between specialists.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Testosterone may influence COVID-19 severity and outcomes.

The document concludes that primary scarring alopecias cause permanent hair loss, have unpredictable outcomes, and lack definitive treatments, requiring personalized care.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

Male pattern baldness affects 38.52% of Asian men in Bangkok, increasing with age and influenced by genes and environment.

VEGF stimulates hair cell growth and increases growth receptor levels through a specific signaling pathway.

Frontal fibrosing alopecia is a type of hair loss that usually happens after menopause.

Frontal fibrosing alopecia may affect nails and could be a type of lichen planus, treatable with certain medications.

Managing frontal fibrosing alopecia and lichen planus pigmentosus is challenging due to resistant hair loss and skin discoloration.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

A rare form of alopecia causes hair thinning without bald spots and may be more common than thought, responding well to steroid treatment.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Autoimmune diseases like lupus, dermatomyositis, and scleroderma can cause hair loss and other hair problems, and treatments for these diseases might also affect hair.

A rare skin condition linked to leukemia improved with chemotherapy.

Use a frontal forelock pattern to manage advanced hair loss.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The KRTAP21-2 gene affects wool length and quality in sheep.

The study concludes that early diagnosis of Frontal Fibrosing Alopecia is important, as it is often found in postmenopausal women, may be related to Lichen Planopilaris, and eyebrow hair loss is a common sign.

Applying InlB321/15 to wounds sped up healing in mice.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Most women with polycystic ovary syndrome (PCOS) have menstrual issues, infertility, acne, and excessive body hair, with the most common type being the non-androgenic phenotype.

Mutations in specific llama genes may affect fiber quality for textiles.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

Oral lichen planus can appear before lichen planopilaris.