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Tigason improved hair growth in a boy with monilethrix without side effects.

Two mouse mutations cause similar hair loss despite different skin changes.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

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

Minoxidil treatment can reduce hair shedding, increase hair volume, and even change hair color in patients with loose anagen hair syndrome.

Caffeine may help hair growth in hereditary hair loss.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Most treatments for hair loss in 1997 were not effective for most people, and maintaining hair growth was difficult.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Genetics, nutrition, lifestyle, and hormones affect early grey hair, but more research is needed.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Hair loss in men is common, treatable, but not curable.

Finasteride and minoxidil are effective for hair regrowth, while treatments for alopecia areata have varying success and continuous treatment is necessary.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Treatment with plasma rich in growth factors improved hair density and thickness for hair loss patients.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Genes and hormones cause hair loss, with four genes contributing equally.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.