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

Frontal Fibrosing Alopecia may be a complex condition linked to hormonal changes in women, not just a form of Lichen Planopilaris.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Media images promote unrealistic beauty standards, affecting body image and eating disorders globally.

Trichoscopy of the beard is useful for diagnosing frontal fibrosing alopecia in men.

Common baldness treatments include cosmetic methods, medication like minoxidil, and surgery, but no cure exists.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

Androgenic alopecia causes hair thinning, and treatments include minoxidil, finasteride, and light therapy.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Synthetic hair implants can cause infection and scarring, so safer options like follicular unit excision are recommended.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

Frontal fibrosing alopecia causes hair loss at the front hairline, and no effective treatment exists.

The document concludes that personalized treatment plans for hair loss in Asian men are necessary and more research is needed to develop effective guidelines.

Tight hairstyles can cause temporary or permanent hair loss, with less hair seen under a microscope in later stages.

Skin diseases look different on pigmented and nonpigmented skin.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Intralesional corticosteroids and 5-alpha-reductase inhibitors are the best treatments for frontal fibrosing alopecia.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Frontal Fibrosing Alopecia in men is often missed and can come with symptoms like facial bumps and hair loss on eyebrows and limbs.

Trichoscopy helps diagnose frontal fibrosing alopecia, even with unusual patterns.