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Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

The study concluded that yellow dots are a common and useful sign for diagnosing alopecia areata in dark-skinned individuals and may indicate the severity of the condition.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Most children with alopecia areata have patchy hair loss and common trichoscopic features like yellow and black dots.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

A man developed an allergic skin reaction after using brimonidine for rosacea.

A man developed an allergic skin reaction to a rosacea treatment and improved after stopping the medication and receiving allergy-specific care.

Alopecia areata patients should have eye check-ups due to increased risk of eye problems.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Trichoscopy can reliably distinguish between alopecia areata and trichotillomania.

Red light therapy temporarily increased blood flow in the eye but didn't change other eye structures.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Taking vitamin B6 corrected a pregnant woman's metabolic disorder, which changed her hair color.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

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

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

Trichothiodystrophy causes unusual hair and developmental issues.

A woman got a skin rash from taking aceclofenac, which went away after she stopped the drug.

Trichoscopy helps diagnose and track treatment for hair loss in men and women.

Skin pigmentation increases in CRPS-affected areas and improves with symptom relief.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Yellow dots are common in severe alopecia areata.