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Some people with primary cicatricial alopecia also have inflammatory bowel disease, suggesting a possible connection.

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

The system can accurately classify hair diseases with 94.5% accuracy using a CNN.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Early detection and intensive treatment of diseases caused by Staphylococcus aureus toxins are crucial for reducing severe health effects.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Parkinson's disease is linked to skin disorders and skin cells help in studying the disease.

Treatment can improve survival and symptoms in dogs with Cushing's disease, but outcomes are unpredictable.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Diagnosing hyperandrogenism in women is complex and requires accurate testing methods and consideration of SHBG levels.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Researchers found two new genetic variants linked to Alzheimer's disease.

Levodopa for Parkinson's disease might be linked to skin issues like melanoma, but it's unclear if the drug or the disease causes them.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Mange in rabbits is a serious disease that can spread to humans and is treated with medications and supportive care.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Skin issues can indicate immune system problems.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.