Search

everythinglearnresearchcommunity

for

Search:↓

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

The document discusses various diseases of the outer ear, categorized by symptoms like redness, crusts, bumps, pus-filled lesions, lumps, ulcers, and hair loss.

COVID-19 may lead to severe skin necrosis without clear underlying causes, as seen in a diabetic patient who required leg amputation.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

Low testosterone levels may contribute to female pattern hair loss in men.

RANKL causes lymph nodes to grow by making certain cells multiply.

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

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.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Using animal names for skin conditions helps with learning and memory.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Metabolic signals and cell shape influence how cells develop and change.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

The right amount of retinoic acid is essential for normal hair growth and development.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.