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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Topical JAK inhibitors may help treat some skin conditions but need more research.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Loss of keratin K2 causes skin problems and inflammation.

Many skin patients also have mental health issues, and doctors should treat both together.

Some skin diseases and their treatments can negatively affect male fertility.

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

Bald men may have a lower risk of testicular cancer.

More research is needed to find the best treatment for dissecting cellulitis of the scalp.

Many patients at a dermatology clinic had scalp problems, often unrelated to why they visited, suggesting scalp checks should be regular.

A girl with symptoms like an autoimmune disorder actually had HIV and a fungal infection, which was hard to diagnose and treat, leading to her death.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Continuous research and innovative strategies are essential for sustainable development.

The conference emphasized innovative solutions for global challenges, including disaster architecture, education, health, and economic impacts.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

It's unclear if COVID-19 vaccination causes SLE; more research is needed.

EPDS is a rare, chronic scalp condition that's hard to treat and needs better awareness for improved outcomes.

Facelift surgery has evolved to focus on natural results and safety, with patient selection and postoperative care being key to success.

Androgenetic alopecia is common in South-West Nigeria, affecting more men than women, with stress worsening the condition.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The new algorithm accurately captures both facial hair and skin in 3D using a camera-based system.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Vitamin B12 deficiency can cause reversible hair color loss in children.