Search

everythinglearnresearchcommunity

for

Search:↓

Oral and maxillofacial surgery has advanced with fluoride reducing tooth decay and high-speed handpieces aiding in more aesthetic procedures, leading to changes in practice and training.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Recent dental research shows diet changes increased tooth decay, red wine reduces bacteria, and dental stem cells can regenerate dentin.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

Edar signaling is crucial for proper hair follicle development and function.

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

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

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

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

Dentin sialoprotein and phosphophoryn are present in rodent hair follicles and may help hair growth and development.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Scientists developed a method to regenerate salivary glands using stem cells.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

Gibbons at Tegal Alur Animal Rescue Center need better feed management to improve their health and weight.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Diagnosing oral ulcers can be complex and requires careful examination and follow-up.

Monilethrix causes short, fragile hair with no specific treatment available.

The conclusion is that certain traits, including perceived facial aging and BMI, are linked to perceived youthfulness differently in men and women.