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Certain micronutrients may improve hair and nail health, but more research is needed to confirm their benefits.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Alopecia Areata has no cure, treatments are limited, and the condition often recurs, but new therapies like JAK inhibitors show promise.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Sulforaphane from broccoli can help protect skin from sun damage.

No single treatment is consistently effective for alopecia areata, and more research is needed.

Menopause reduces skin collagen and elasticity, and while estrogen therapy can help, its risks require careful consideration.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Disruptions in hair follicle fibroblast dynamics can cause hair growth problems.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

IGF-1 may affect hair growth and loss, but more research is needed to confirm effective and safe treatments.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

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.

Most hair loss disorders can be accurately diagnosed and treated in an outpatient setting.

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.

Some skin diseases and their treatments can negatively affect male fertility.

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

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.