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Dogs with zinc-responsive dermatosis need zinc supplements or dietary changes for treatment.

Testosterone can slow down hair growth when combined with certain cells from bald scalps, and this effect can be blocked by an androgen receptor blocker.

Dihydrotestosterone (DHT) stops hair growth in mice by lowering a growth factor important for hair.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Cholesterol-related compounds can stop hair growth and cause inflammation in a type of scarring hair loss.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Blocking EGFR can cause skin inflammation by disrupting IL-1 signaling.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Sodium metabisulfite increases sodium channel activity, leading to higher cell excitability and potential damage.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Insulin resistance can lead to skin problems like acne and psoriasis.

Eruptive vellus hair cysts are often missed in diagnoses.

Almost 40% of women aged 20-70 in Isfahan had hair loss, with it being more severe in those with low ferritin levels.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

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

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Mutations in the LIPH gene cause woolly hair in a child.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.