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

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.

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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.

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.

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

Dr. Rochelle Torgerson says female-pattern hair loss is often hereditary, starts after puberty, and can be slowed with treatments like Minoxidil. It can also indicate other health issues.

Androgenetic alopecia (AGA) is a common, hereditary hair loss condition that can be slowed but not permanently reversed with available therapies.

Some treatments for hereditary hair loss are effective but vary in results and side effects; new therapies show promise but need more research.

Common baldness is a hereditary condition that can be treated with medications or surgery to prevent progression and improve self-esteem.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Caffeine may help hair growth in hereditary hair loss.

Light therapy might help treat hereditary hair loss by improving hair follicle growth in lab cultures.

New treatments are being explored to slow or reverse hereditary hair loss.

Female hair loss is often hereditary and can be treated with medication, hair transplants, and lasers.