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Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Reconstruct lips with proper planning, templates, and revisions for appearance and function.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

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

Hair loss improved with treatment and successful transplant.

Pannexin 3 is important for bone formation and the development of bone cells.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

FGF13 gene changes cause excessive hair growth in a rare condition.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

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

A child with a rare vitamin D-resistant condition improved with treatment.

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

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

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.

Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

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

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

Some skin diseases and their treatments can negatively affect male fertility.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

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

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.