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A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Almost all patients with chronic kidney disease not yet on dialysis have at least one skin problem.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Platelet-rich gel is an effective treatment for healing scalp wounds with exposed skull.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Hair examination helps diagnose rare neurological diseases in children.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A boy with a rare skin condition improved quickly after starting zinc supplements.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

The new model detects hair clusters more accurately and efficiently, helping with early hair loss treatment and diagnosis.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Chemokine signaling is important for hair development.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The fuzzy gene is crucial for controlling hair growth cycles.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Artificial hair implants can cause severe skin problems, often needing surgical removal.

The book helps surgeons improve hair transplants for Asian patients.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Vitamin B12 deficiency can cause reversible hair color loss in children.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.