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

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Common acne treatments can cause various side effects, like skin irritation and more serious issues, but combination therapies are often more effective and better tolerated.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Pannexin 3 is important for bone formation and the development of bone cells.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Some skin diseases and their treatments can negatively affect male fertility.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Hair loss improved with treatment and successful transplant.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

Skin changes can indicate starvation and nutritional deficiencies in anorexia nervosa.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Some skin medications are safe during pregnancy and breastfeeding, but others can harm the baby and should be avoided.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Stem cell therapies show promise for hair regrowth in androgenetic alopecia.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Edar signaling is crucial for controlling hair growth and regression.

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

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.