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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Probiotics help reduce hair loss and increase hair growth in people with androgenic alopecia.

Personalized medicine in dermatology uses molecular biomarkers to improve diagnosis and treatment but needs further advancements for practical use.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

New findings may help diagnose and understand scarring alopecia better.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The rash on the infant indicated a serious underlying condition.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Scalp melanoma is more common and easier to diagnose early in people with androgenetic alopecia due to sun damage.

Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.

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

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Microneedles are effective for painless drug delivery and promoting wound healing and tissue regeneration.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Tiny vesicles from stem cells could be a new treatment for healing wounds.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

New treatments like nanotechnology show promise in improving skin cancer therapy.