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A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Epidermal nevi are skin cell clusters linked to various syndromes.

The FUE technique can effectively restore moustaches in patients with cleft lips and alopecia, with few complications.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

A gene mutation causes woolly hair in a Syrian patient.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Minoxidil effectively treats hair loss, works better for women, and requires consistent use.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

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

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

The document concludes that the trichogram is a useful tool for diagnosing hair loss and suggests semi-organ cultures for practical trichological research.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Blocking JAK-STAT5 signaling in mice leads to hair growth.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

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

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

New treatments for hair loss show promise, especially finasteride for men and a stronger minoxidil formula.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Taking Propecia might lead to the development of cataracts.

The document concludes that proper diagnosis and evidence-based treatments are crucial for managing hair diseases, and psychological support for patients is important.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Pili anulati may cause hair loss, proper diagnosis and treatment needed.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Finasteride, often used for hair loss, can potentially cause cataracts.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.