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

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

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

Pattern hair loss is mainly caused by genetics and hormones, with limited effective treatments available.

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

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

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The chapter explains causes of hair loss and excessive hair growth in animals.

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

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.

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

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

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

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.

Effective treatments for hair loss are a major focus in dermatology.

Dermal papilla cells play a key role in hair loss by responding to androgens.

Gene therapy with a vitamin D receptor gene improved hair growth in rats with a type of rickets-related baldness.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Alopecia, or hair loss, can be caused by genetics, illness, or certain drugs, and can be treated with synthetic or natural medications.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Androgenic alopecia is a type of hair loss that's partly inherited and can be due to hormonal imbalance.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Some people with alopecia areata, a hair loss condition, get better within a year without treatment, but it can happen again.

Female pattern hair loss is common, often starts in the 30s or 40s, worsens after menopause, and can negatively affect quality of life.

A new food supplement was highly effective in curing hair loss in young men.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.