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Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Vitamin D3 ointment improved skin bumps on the chin but didn't give lasting results after stopping use.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A woman's hair loss, resembling an autoimmune condition, improved after treatment, but requires ongoing checks due to potential serious associations.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Obesity is linked to skin conditions like acanthosis nigricans and skin tags, which may indicate high insulin levels.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

Some hair loss disorders cause permanent loss due to scarring, and treatments like steroids don't always work well.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Acne is caused by increased sebum, abnormal skin shedding, bacteria, and inflammation, not dirt; treatments vary from creams to antibiotics or isotretinoin, with severe cases needing a dermatologist's care.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

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

New imaging techniques can assess and track changes in mouse acne without harm, aiding treatment choices.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

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

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

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

Light microscopy is useful for diagnosing different hair disorders.

The dog likely has a condition similar to Canine alopecia X.

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

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Some people with pattern hair loss may also have scalp inflammation and scarring similar to lichen planopilaris.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.