Search

everythinglearnresearchcommunity

for

Search:↓

ViviScal®, a food supplement, was found to be highly effective in treating hereditary hair loss in young males, while fish extract showed no impact.

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

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

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.

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

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

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

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

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

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

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

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.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

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.

Tranexamic acid effectively reduced swelling episodes in a girl with a rare form of hereditary angioneurotic edema.