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Accidentally eating a topical steroid may rarely cause acute generalized pustular psoriasis.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Aromatase gene variation may increase female hair loss risk.

Androgenic steroids can slow down or stop the growth of certain skin fungi.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

There are many treatments for permanent hair loss disorders, but their effectiveness varies and there's no clear best option.

Systemic diseases can cause hair loss, which is often reversible with treatment.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

The most common skin problems in Indian children are infections and eczemas.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Glycerol is essential for skin hydration in mice without sebaceous glands.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

Androgens, like DHT, affect hair growth and treatments like finasteride may help.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Tissue environment greatly affects the unique epigenetic makeup of regulatory T cells, which could impact autoimmune disease treatment.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.