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Relatives of women with PCOS symptoms are more likely to have similar health issues.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

Recent selection on immune response genes was identified across seven ethnicities.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Arctiin helps protect hair cells from damage and death caused by oxidative stress.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Light microscopy is useful for diagnosing different hair disorders.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Some skin diseases and their treatments can negatively affect male fertility.

Early diagnosis and treatment of PCOS in young people is important to prevent long-term health problems.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

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

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The document concludes that early diagnosis and treatment of PCOS in teenagers is important for managing symptoms and preventing long-term health problems.

PCOS may have evolved as an advantage in past environments with food scarcity.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A new mouse mutation causes skin and hair defects due to a gene change.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.