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New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A new gene mutation linked to a skin condition was found in a Spanish family.

Some COVID-19 patients have different skin problems, which might be the only sign of the virus or related to other health issues.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

People with alopecia areata are more likely to get migraines, and vice versa.

Wound healing is greatly affected by the types of bacteria present, which can either help or hinder the process.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

EGFR inhibitors cause skin issues and hair loss by weakening skin defenses, suggesting antibiotics and targeted treatments can help.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

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

The document says that understanding the causes of PCOS is important for treatment, especially in distinguishing the syndrome from just having cystic ovaries, and that losing weight is key for obese women with PCOS.

Using three different drugs together may better treat eye diseases like glaucoma and macular degeneration.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Cancer treatments often cause hair disorders, significantly affecting patients' quality of life, and better management methods are needed.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Ifidancitinib, a JAK inhibitor, effectively regrows hair in mice with alopecia by tiring out harmful T cells.

CTE and FPHL are different hair loss types with unique causes.

Some women with PCOS have rare genetic variants linked to the condition.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Homoeopathy has helped treat hair loss after Covid-19, considering the patient's overall condition.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Dogs with ear infections have a higher rate of yeast infection, especially German Shepherds, with seasonal variations observed.

Rosacea is a skin condition with unclear causes, classified into four subtypes.

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

Male pattern baldness involves hormones and cell signals affecting hair growth.

Corticosteroid treatment reduces inflammation and alters hair keratins in alopecia areata.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Post-finasteride patients show changed neuroactive steroid levels, possibly causing erectile dysfunction and depression.