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People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Mutations in the KRT85 gene cause hair and nail problems.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Photobiomodulation effectively treats hair loss in dogs with black hair follicular dysplasia.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

The mineralocorticoid receptor may play a role in skin and hair health and could be a new target for treating related disorders.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Sandalore® improves hair growth and quality in people with hair loss.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

Twins had rare skin cysts likely due to genetics.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.