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The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Taking He Shou Wu (Polygonum multiflorum) caused liver injury in a woman using it for hair loss.

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.

Cicatricial alopecia causes permanent hair loss and is treated to relieve symptoms and stop progression.

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.

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

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

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.

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

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

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.

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

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

Hormonal differences affect male pattern baldness.

Skin problems like excessive hair growth, acne, and dark skin patches can be signs of Polycystic Ovarian Disease, which may also be linked to family history and a risk for diabetes.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

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

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

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

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Early recognition and management of connective tissue diseases like lupus are crucial in young patients.

Early diagnosis and treatment, using finasteride, minoxidil, or hair transplantation, improves hair loss outcomes.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.