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Recognizing LET and AITD can help diagnose SLE early for better treatment.

A 10-year-old girl had genital pain from a small, red, crusty mass on her labia.

The over-the-counter supplement DHEA could make COVID-19 worse, especially in diabetics and people with G6PD deficiency.

Long-term use of azole antifungals can cause hair loss, hormonal imbalances, and severe skin reactions.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

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

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

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

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

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

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

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

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

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

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

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

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

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

The study suggests that treating early hair loss with Nourkrin® with Marilex® can help prevent further hair loss and may be linked to reducing the risk of lifestyle diseases.

Hair changes can indicate systemic diseases or medication effects.