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Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

Younger people are at a higher risk for Fibrosing Alopecia in a Pattern Distribution than previously thought, with common symptoms and possible involvement of mast cells in its development.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

A 3-year-old girl has a rare condition causing sparse hair and nail issues, with minimal improvement from treatment.

FAPD is a possible diagnosis for hair loss in patients of color and requires multiple evaluations for accurate diagnosis.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

Hair-related body dysmorphic disorder is common in hair loss patients and needs early recognition for proper treatment.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Tinea faciale can be mistaken for lupus due to similar symptoms.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Women with Frontal Fibrosing Alopecia have more wrinkles near their ears than similar aged women without the condition.

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

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

Hair diameter difference, brown skin discoloration around hair follicles, and missing hair in certain areas are key signs of androgenetic alopecia (commonly known as hair loss) when viewed under a dermoscope.

Facial feminization surgery helps make facial features more feminine, improving patient satisfaction and safety.

Two young siblings experienced hair loss without hormone issues or other skin problems.

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

The study suggests fibrosing alopecia in a pattern distribution has distinct features and may vary by race.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Frontal fibrosing alopecia mainly affects women over 50, causing hair loss and specific skin changes.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Frontal fibrosing alopecia is increasingly affecting men, causing hair loss around the hairline and possibly other areas.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

The girl has a genetic hair condition causing thin hair since childhood.

Antifungal treatment can improve severe skin infections with cutaneous horns.

Daughters with affected mothers may develop frontal fibrosing alopecia early.