Search

everythinglearnresearchcommunity

for

Search:↓

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Experts met to improve care for ichthyosis patients in Spain.

Treating hair loss effectively may require a multi-sided approach, using different treatments together, and topical treatments could be more effective and safer than oral ones.

IRS-specific genes in Tan sheep hair follicles peak at birth and may affect wool crimp.

Experts recommend personalized treatment plans for best outcomes in managing Alopecia Areata.

Six genetic conditions are often linked to complete scalp hair loss in children.

Cactus extract from Notocactus ottonis may help promote hair growth.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

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

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

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.