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Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The Hairless gene is crucial for healthy skin and hair growth.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

New treatments focusing on immune pathways show promise for stubborn hair loss.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Knocking out certain genes in mice helps understand skin and hair growth problems.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.