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Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

The document explains how to identify different hair problems using a microscope.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Nanomaterials in biomedicine can improve treatments but may have risks like toxicity, needing more safety research.

The study suggests that acne keloidalis nuchae is linked to conditions like pseudofolliculitis barbae, scalp infections, metabolic syndrome, and is more common in males with an average onset age of 25.4 years.

Finasteride given to baby rats causes anxiety-like behavior and worsens learning from punishment in adult rats.

Using neurohormones to control keratin can lead to new skin disease treatments.

An enzyme other than TNAP might be responsible for vitamin B-6 metabolism in the skin.

Spermidine helps protect against aging by preserving telomere length.

Treat adult facial vascular anomalies with lasers, surgery, or observation, depending on the patient's specific condition.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

The type 3 IP3 receptor is important for controlling hair loss and growth.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A woman's rare adrenal tumor caused high testosterone and cortisol levels, which normalized after the tumor was removed.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Cantú syndrome may be linked to pituitary adenomas.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

The ketogenic diet can worsen biotin deficiency, suggesting a need for biotin supplements.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

The document concludes that hormone therapy is essential for treating gender dysphoria, with specific drugs and monitoring protocols recommended for safety and effectiveness.

Dogs with sex hormone imbalances may not drink or pee a lot but often lose hair on their body and can have reproductive system issues.