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The study concluded that yellow dots are a common and useful sign for diagnosing alopecia areata in dark-skinned individuals and may indicate the severity of the condition.

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

Early hair loss links to metabolic issues in young Indian men.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Special immune cells called Treg cells are important for maintaining and regenerating hair by activating a specific growth signal in hair stem cells.

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

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

Environmental factors like temperature and nutrition affect hair growth, with humans showing seasonal hair growth differences.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Low-dose oral isotretinoin improved hair loss and facial bumps in patients with a specific type of hair loss.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Chromium salts may help with insulin sensitivity in PCOS, but more research is needed to confirm their overall effectiveness and safety.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Red and infrared light therapy improves hair growth in balding patients.

The paper concludes that for natural-looking hair restoration, it's important to create an irregular hairline, use appropriately sized and angled grafts, and ensure a snug fit between grafts and recipient sites.

A 6-year-old girl with alopecia universalis regrew most of her hair after treatment with simvastatin/ezetimibe, minoxidil, and prednisolone.

A patient with Ehlers-Danlos Syndrome improved after treatment for fat malabsorption and essential fatty acid deficiency.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A girl with red hair developed hair-pulling and body image disorders after being bullied for her hair color.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

Some breast cancer treatments caused long-term hair loss in women, similar to a condition called alopecia areata.

The girl has a genetic hair condition causing thin hair since childhood.

Mutations in the P2RY5 gene cause hereditary woolly hair.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

The document concludes that skin aging in women can be caused by UV exposure and hormonal changes, and treatments like hormone replacement therapy and various skin therapies can help.