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The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Low DHEA-S levels might be linked to alopecia areata and could be a potential treatment target.

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

A new gene variant causes glucocorticoid resistance in a mother and son.

Free fatty acids may increase androgen production, potentially contributing to polycystic ovary syndrome.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Cyclosporine can cause a unique skin condition called "cyclosporine-induced folliculodystrophy."

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.

A special diet can significantly reduce skin problems in dogs.

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.

Common skin fungal infections can suggest a weak immune system, and for scalp infections, pills work better than creams, with several drug options available.

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.

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

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