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A man's skin condition and poor diet led to a scurvy diagnosis.

Obesity is linked to various skin conditions and issues, and losing weight can improve these conditions.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Obese people are more likely to have certain skin conditions like dark patches, stretch marks, skin tags, and bumpy skin.

The woman's skin and hair symptoms were confirmed as frontal fibrosing alopecia, and while facial papules are common in such cases, there's no effective local treatment, but systemic treatments can help.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Traumatic anserine folliculosis is a harmless skin condition in young males that needs correct diagnosis to avoid unnecessary treatments.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Obese people have more skin problems like stretch marks and infections, which get worse with higher obesity levels.

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

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

The conclusion is that there's a link between high testosterone levels, insulin resistance, and certain skin conditions, regardless of obesity.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Nilotinib can cause keratosis pilaris, a skin condition.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

KFSD causes scarring hair loss and skin roughness, mainly in males.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Vemurafenib causes significant skin side effects, requiring regular dermatologist care and sun protection.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Wnt3a protein, when packed in liposomal vesicles, can stimulate hair growth and could potentially treat conditions like hair loss.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Being overweight can cause or worsen skin problems in children, some more common in darker skin, and is often linked to insulin resistance.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.