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Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

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

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Combining PRP injections with minoxidil 2% effectively promotes hair growth in hereditary hair loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Minoxidil helps 32% of patients with hereditary baldness regrow hair.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Using minoxidil on the scalp can help grow hair for people with hereditary baldness.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new mutation in the HR gene causes hair loss in a specific family.

Monilethrix is a rare genetic hair disorder that's hard to treat.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

Some treatments like minoxidil, finasteride, and surgery can help with hereditary hair loss.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Mutations in hKAP1 genes may cause hereditary hair disorders.

The document concludes that scalp disorders can be treated with hair washing, specific shampoos, medications, and sometimes surgery or hair transplants, but hereditary baldness is untreatable.

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

Baldness is often hereditary and linked to male hormones, becoming noticeable when half the hair is lost.

Mutations in the P2RY5 gene cause hereditary woolly hair.