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Experts met to improve care for ichthyosis patients in Spain.

Certain existing drugs, like glycopyrronium and botulinum toxin type A, may help treat excessive sweating.

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

Monitoring new epilepsy drugs after they're sold is crucial to find rare and long-term side effects that initial tests might miss.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Diabetes can cause a variety of skin disorders, some of which may signal more serious health issues.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

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

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Alopecia areata patients have varied cancer risks, with some cancers being lower and others higher.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

FGF13 gene changes cause excessive hair growth in a rare condition.

Gene linked to common hair loss found, may lead to new treatments.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.