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The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Longer CAG repeats in gene linked to more severe hair loss in females.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

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

The first pediatric case of naevus trichilemmocysticus was documented.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Less than a quarter of alopecia areata cases were unusual forms or had paradoxical regrowth.

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

Most women with hyperandrogenism first show acne, and skin conditions like hirsutism and acanthosis nigricans are good indicators of the condition.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Inflammatory skin conditions are the most common in Brazilian children, with atopic dermatitis being the top issue.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.

Newly divided skin cells quickly move to join skin structures due to tissue tension and specific signals.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.