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A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Pregnancy can cause skin changes and affect existing skin conditions, with limited treatment options due to the need for fetal safety.

The document concludes that clinicians should be aware of common hair and scalp disorders in women of African descent and that more research is needed to develop effective treatments.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Stem cells and their surrounding environment in hair follicles work closely together, affecting hair growth and having implications for cancer and tissue regeneration.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

Indole-based compounds improved ovarian health in rats with PCOS, with L-Tryptophan and Tryptophol being most effective.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

Immunosuppressive therapy helps manage autoimmune diseases but carries risks like infection and potential for malignancy.

Low serum ferritin levels are linked to hair loss in women.

Dissecting Cellulitis of the Scalp is more common in young men and often associated with head and neck acne.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Understanding fetal skin development helps diagnose congenital skin diseases.

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

Glucocorticoids affect dogs' skin reactions to histamine, which vary by time of day.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Melatonin may benefit skin health and could be a promising treatment in dermatology.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Zaleya pentandra extracts, especially acetone, may be useful for new medicines and food industry applications.

The immune system plays a key role in tissue repair, affecting both healing quality and regenerative ability.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.