Search

everythinglearnresearchcommunity

for

Search:↓

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

NFIC helps rat dental cells grow and turn into bone-like cells.

Traditional Chinese Medicine and biomaterials help heal chronic wounds by targeting multiple pathways.

Platelet-rich plasma is as effective as mineral trioxide aggregate for pulp capping and may offer better cellular responses.

The scaffold could effectively replace traditional methods for bone regeneration in dental applications.

Keratin could help create enamel-regenerating toothpaste in a few years.

MSC-protein helps regenerate gum tissue and bone.

Platelet concentrates are useful for tissue repair in medicine and dentistry, with L-PRF showing promising results in various treatments.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Mothers and newborns with dental fillings have higher mercury in their hair, but adding fillings during pregnancy doesn't raise mercury levels further.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Younger patients with severe alopecia areata often have nail problems.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

A 12-year-old boy has a rare, harmless hair loss on his chin with no need for treatment.

Mutations in the HOXC13 gene cause hair and nail development issues.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.

A 16-year-old girl with gum overgrowth and excessive hair growth had successful gum surgery and healed well.

Advances in genetics may lead to targeted treatments for hair disorders.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

A baby's toe was severely damaged by a hair tourniquet, leading to bone and tendon damage, but improved after surgery and treatment.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Many alopecia patients have undetected thyroid abnormalities that can be found through physical exams.