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Vitamin D has potential benefits for cancer prevention, heart health, diabetes, obesity, muscle function, skin health, and immune function, but clinical results are mixed and more research is needed.

Sex hormones affect hair and feather growth and may help manage alopecia and hormone-dependent cancers.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

The document concludes that there is a need for more research and regulation in dermatology, covering topics like latex allergy in children, the use of botulinum toxin, and treatments for skin conditions.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Only a few hair-specific keratins are linked to inherited hair disorders.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

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

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

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

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

A specific gene mutation causes congenital hair loss.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

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

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.