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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.

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

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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

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

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

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

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

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

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

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

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.

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

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

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

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

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.