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People with Alopecia Areata have more herpes simplex infections but similar rates of cancer, blood clots, and heart disease compared to those without it.

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.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

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

Skin problems are very common in people with end-stage kidney disease.

Fluridil safely promotes hair growth in men with androgenetic alopecia.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Fluridil safely promotes hair growth in men with androgenetic alopecia.

Certain types of T cells are essential for healthy skin and play a role in skin diseases, but more research is needed to improve treatments.

PRP injections may be a safe, effective alternative for hair loss treatment compared to minoxidil and finasteride.

Finasteride may cause suicidal thoughts and mental side effects, especially in young people with hair loss.

The document concludes that "Dictamnus" has a rich cultural history and potential as a herbal medicine, warranting more research into its effects and safety.

Hirsutism is common body hair growth due to genetics and hormones, and while not a disease, it can be distressing; virilisation includes hirsutism with other male traits and needs medical attention.

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

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

Laser treatment and deroofing are effective options for hidradenitis suppurativa.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Pulsed dye laser and hydrogel dressings effectively treat hypertrophic scars.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The letters discussed medical tools, costs, treatment efficacy, and patient care complexities.

Minoxidil treats high blood pressure and side effects can be managed.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

Understanding how acne develops in different diseases could lead to new treatments.

STK11 gene polymorphism does not predict metformin response in PCOS.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.