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Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

Trichoscopy helps diagnose and monitor the treatment of fungal scalp infections in children.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

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

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Epigenetic factors play a crucial role in skin health and disease.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Combining FUE hair transplantation with PRP improves hair density and patient satisfaction in scarring alopecia.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Examining nail biopsies is useful for diagnosing nail diseases.

FOXO1 is important for wound healing, but its dysfunction in diabetes can slow the healing process.

No CD44 in alopecia areata, present in normal and androgenetic alopecia.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

Alopecia areata is an autoimmune disease causing hair loss, treatable with immune-modulating drugs, and linked to genetics.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

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

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