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miR-199a-3p controls hair growth and is linked to alopecia areata.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Successful outcomes depend on accurate diagnosis and strong doctor-patient relationships.

Iron deficiency can cause psychiatric symptoms that improve with proper treatment.

Botulinum toxin A has limited effectiveness for 3 months in treating female pattern hair loss and may reduce scalp oiliness.

PRP therapy with minoxidil is more effective for hair growth than PRP alone.

Hair loss due to scarring can be treated by reducing inflammation, removing scar tissue, and transplanting hair. The Follicular Unit Extraction technique is effective but requires skill and time. Future focus should be on scar-less healing methods.

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

An 11-year-old girl with a hair-pulling disorder had a hairball in her stomach and was treated with medication, therapy, and a team of doctors.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Diagnosing diffuse alopecia, a hair loss condition, can be challenging and may require a scalp biopsy or tracking the disease's progression when symptoms and skin tests aren't enough.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Ischemic modified albumin could be a new indicator of oxidative stress in people with alopecia areata.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Experts advise using sunscreen and proper skin care before, during, and after procedures to speed healing, prevent complications, and reduce scarring.

Non-surgical treatments like thread lifts, PRP therapy, HIFU, and radiofrequency effectively rejuvenate and tighten facial skin.

Platelet-rich plasma (PRP) shows promise in skin and hair treatments but results vary with preparation methods.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Higher CD70 and CD27 gene expression in alopecia areata lesions predicts disease severity and activity.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

Combining TRA and latanoprost is most effective for treating localized alopecia areata.

Autologous platelet concentrates show promise in esthetic treatments but need more standardized research.

Low-dose oral minoxidil is safe for treating children's hair disorders.

Adipose-derived stem cells can help repair and improve eye tissues and appearance.

Proper planning and technique in upper-face feminization surgery are crucial to avoid complications and revisions.

New treatments for hair loss should target eight main causes and use specific plant compounds and peptides for better results.