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Different ethnic groups have unique hair growth patterns, with African hair growing slower and less dense, Asian hair growing fast but sparse, and Caucasian hair being densest; men are more likely to experience hair loss than women.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

The procedure is effective for reducing the forehead despite potential for visible scars.

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.