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Frontal fibrosing alopecia can cause sudden hair loss on limbs, similar to scalp hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Leg hair transplants can create a natural-looking hairline and show successful growth over several years.

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

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Androgenetic alopecia is a common hair loss condition caused by testosterone effects on hair follicles, leading to thinner, shorter, and less pigmented hair, diagnosed using scalp dermoscopy and treated with topical minoxidil, antiandrogen agents, and 5-alpha reductase inhibitors.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

New techniques in hair restoration surgery can fix unnatural results from old methods, improving patient self-esteem.

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

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

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

The surgical technique of scalp advancement and pretrichial brow lift shortens the forehead and lifts brows, is good for women and transgender women with high foreheads, but not recommended for men and has some risks.

Most patients with frontal fibrosing alopecia are middle-aged women, often have thyroid disease, and some treatments can help stabilize the condition.

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

Men and women have different hairline restoration needs, with natural design being more complex for women, and hairline changes being important for transgender individuals' transitions.

Michael L. Beehner proposed a standardized way to describe balding areas on the scalp to help hair restoration experts communicate better.

The CORIN gene variant causes the golden color in Siberian cats.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

In 2002, hair restoration improved by using a different area for grafts and absorbable sutures, leading to less discomfort and better results.

New genetic mutations linked to rare skin disorders were found in three newborns.

The document concludes that using autologous follicular unit implantation is a successful method to correct hairline deformities after facial rejuvenation.

JAK inhibitors help hair regrowth but not fully effective for androgenetic alopecia.

Most Spanish Caucasian women have a widow's peak, and their hormone levels suggest they process certain hormones faster.

Different women have various natural hairline shapes, and understanding this is important for designing hair transplants.