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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Genetic defects and UV radiation cause skin damage and aging.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

Knocking out certain genes in mice helps understand skin and hair growth problems.