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Mutant mice help researchers understand hair growth and related genetic factors.

FFA's causes may include environmental triggers and genetic factors.

The document concludes that clinicians should be aware of common hair and scalp disorders in women of African descent and that more research is needed to develop effective treatments.

Pigmented casts are common in several hair loss conditions and can help diagnose specific types of alopecia.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

Chronic inflammatory skin diseases are caused by disrupted interactions between skin cells and immune cells.

Scalp biopsy helps tell apart permanent and temporary hair loss types and guides treatment.

Afro-textured hair is more fragile and prone to certain scalp conditions, requiring careful treatment and more research for effective management.

Certain microRNAs might help identify and understand Frontal Fibrosing Alopecia.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

A JAK inhibitor improved both severe hair loss and chronic skin disease in one patient.

The text talks about a rare skin condition causing hair loss and suggests that people with this should also check their lung and heart health.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

New targeted immunotherapies are improving treatment for inflammatory skin diseases.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

SLE should be considered in unexplained fevers, even in males.

People with atopic dermatitis have different skin bacteria, and targeting these bacteria might help treat the condition.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

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.

Taking Propecia might lead to the development of cataracts.

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.

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

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.