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The marine complex supplement significantly improved hair growth in men with thinning hair without adverse effects.

Cosmetic surgery is more popular and cost-effective, but outcomes depend on the surgeon's skill and all procedures have potential complications.

Most people with hypothyroidism have skin problems like dry skin and hair loss.

Mutant mice help researchers understand hair growth and related genetic factors.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Family-based treatment is the best outpatient care for stable teens with anorexia, and more research is needed on medication and treatment effectiveness for young people with eating disorders.

Cytokines are important for immune responses and treating diseases, but they can cause side effects like fever and skin issues.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

New cancer drugs can cause skin side effects like rashes, dry skin, hair changes, and nail problems.

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.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

People with HIV and low T cell counts have more hair and scalp problems.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

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

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Hair usually grows back 1-3 months after treatment for anagen effluvium, and children with Loose Anagen Hair Syndrome often improve by adolescence.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The dietary supplement significantly improved skin, nails, and hair in older adults.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.