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Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Pregnant women often experience skin and hair changes, with over half getting stretch marks and pigment changes, and should be cautious with cosmetic procedures due to potential risks.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Six genetic conditions are often linked to complete scalp hair loss in children.

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

Alopecia areata in Taif is common, mainly immune-related, and best treated with topical corticosteroids and vitamins.

Skin changes are key for early diagnosis and treatment of rheumatic diseases.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Skin changes in women with PCOS are mainly due to hormonal imbalances.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Aging causes hair to gray and thin, with the timing of graying varying by race, and factors like oxidative stress and genetics can lead to hair loss.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Menopause often leads to lower sexual desire and discomfort during sex, but treatment should be personalized and only if it bothers the woman.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Delayed ejaculation is a complex issue caused by psychological, biological, and lifestyle factors, requiring a holistic treatment approach.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Targeted cancer therapies often cause skin reactions, so dermatologists must manage these effects.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

IL-2 treatment causes skin eruptions and other reversible side effects, and may play a role in psoriasis.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.