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Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Laser hair-comb therapy doesn't improve male-pattern hair loss.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Lamins are vital for cell survival, organ development, and preventing premature aging.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Notch-related genes play a key role in the development and cycling of hair follicles.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Insulin resistance and high male hormone levels are major causes of Polycystic Ovary Syndrome.

New targets for making and using brain-synthesized steroids could lead to better treatments for brain disorders and alcoholism.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

Melatonin affects certain genes and pathways involved in cashmere goat hair growth.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

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.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

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

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

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.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.