Search

everythinglearnresearchcommunity

for

Search:↓

Tailor treatments for vitiligo to patient needs for best results.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The document explains the genetic causes and characteristics of inherited hair disorders.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

Non-invasive methods can effectively diagnose and manage alopecia areata.

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

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

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

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

The conclusion is that accurate diagnosis of different types of hair loss requires good teamwork between skin doctors and lab experts.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

Gonadal dysgenesis, like Turner's and Klinefelter's syndromes, negatively affects bone health, but hormone treatments can help.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Some breast cancer patients developed permanent hair loss after chemotherapy and hormonal therapy, showing patterns similar to common baldness and alopecia areata.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.