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The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

Early diagnosis and strong corticosteroids are crucial for managing lymphocytic cicatricial alopecia.

Alopecia areata patients have eye issues and need regular eye exams.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

Stopping minoxidil and using prostaglandin analogues improved the man's eye condition.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

A specific gene mutation causes sparse, brittle hair in a family.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

Finasteride helps treat eyelid spasms.

Sebaceous glands are often preserved and PPARy expression is constant in some cases of Central Centrifugal Cicatricial Alopecia.

Minoxidil can cause a rare eye condition, but it was successfully treated with oral Eplerenone in one case.

A 39-year-old woman developed uncombable hair syndrome after taking oral contraceptives.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

The patient has a rare skin condition that shows features of two known disorders.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Recognizing unusual symptoms can lead to early diagnosis and effective treatment of systemic lupus erythematosus.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.