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Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Hair loss, known as Androgenetic Alopecia, is often caused by hormones and can be diagnosed using noninvasive techniques. Treatments include topical minoxidil and oral finasteride, with new treatments being explored. There may also be a link between this type of hair loss and heart disease risk.

Dermal papilla cells can help regrow hair and are promising for hair loss treatments.

Stem-cell therapy shows promise for skin conditions but needs more research.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

Different types of fibroblasts play various roles in kidney repair and aging, and may affect chronic kidney disease outcomes.

Sunflower oil was found to promote hair growth in mice with hormone-induced hair loss.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

Human stem cells can help form hair follicles in mice.

People with ectodermal dysplasias often have reduced saliva production and should get saliva tests.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

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

Tissue expansion successfully treated alopecia in a child with hypohidrotic ectodermal dysplasia.

Mutations in the KRT85 gene cause hair and nail problems.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

Neonatal hair can help determine drug exposure during pregnancy.

Human sweat glands have a type of stem cell that can grow well and turn into different cell types.

Platelet-rich plasma (PRP) is a simple, cost-effective treatment that promotes hair growth and reduces hair loss, with high patient satisfaction.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.