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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Trichotillomania is more common than previously thought, with increasing diagnosed cases.

Erosive pustular dermatosis of the scalp is a rare condition that causes scarring hair loss, mainly in older women, and requires ongoing treatment.

Seborrheic dermatitis and dandruff are often treated with antifungal and anti-inflammatory medications, which can reduce symptoms and yeast growth on the scalp.

Ketoconazole cream is effective for skin conditions like seborrheic dermatitis and may help with hair loss and other skin issues, with generally mild side effects.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

An infant with scalp fungus was cured after extended treatment with antifungal medication.

People with allergies or high eosinophil levels have a higher chance of severe hair loss from alopecia areata, and sudden hair loss can indicate chronic graft-versus-host disease.

Some antiseizure medications can cause cosmetic problems like hair loss, excessive hair growth, acne, and gum overgrowth.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Certain gene variations might be linked to severe acne in women but not in men.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.

Hair amino acid levels can indicate metabolic disorders.

Most skin conditions can be managed with general medical knowledge.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

The hair of two ancient Chilean mummies is well-preserved and contains high levels of heavy metals.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The document explains how male reproductive hormones work and affect the body.

An imbalanced gut and lack of biotin can cause hair loss in mice.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.