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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.

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

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

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

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

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

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

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

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

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

Vitamin D3 affects cell differentiation in specific skin areas.

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

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

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

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.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Mutations in the P2RY5 gene cause hereditary woolly hair.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Using minoxidil on balding scalps can stimulate hair regrowth and increase blood flow. It's an effective treatment for early hair loss.

Eating high glycemic foods and drinking milk may worsen acne by increasing insulin and IGF-1 levels.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Hair loss discovery causes stress; talking to dermatologists helps.

The book "Hair Science and Technology" provides a deep understanding of hair biology and genetics, discusses hair growth, density, and diseases, and offers methods for managing hair loss and caring for hair growth.