Search

everythinglearnresearchcommunity

for

Search:↓

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Two siblings have a rare genetic condition causing curly, coarse hair.

Woolly hair is a rare genetic condition with no effective treatments.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

To diagnose hair loss, use a systematic approach including history, exams, and tests.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

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

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

PRP helps hair growth in common hair loss disorder.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.