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Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

Genetic variations affecting skin structure play a key role in severe acne.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Zinc can help with some skin problems, but its effectiveness varies depending on the condition.

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.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Taking too many vitamin and mineral supplements can cause serious health problems.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

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

The Hairless gene is crucial for healthy skin and hair growth.

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

The document concludes that various skin conditions have specific treatments, ranging from antihistamines for urticaria to surgery and medication for tumors and chronic skin diseases.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

A gene mutation in Lama3 is linked to a common type of hair loss.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Four specific genes are linked to keloid formation and could be potential treatment targets.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.