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Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

Finasteride, often used for hair loss, can potentially cause cataracts.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Reflectance confocal microscopy reliably identifies skin cancer features like horizontal skin tissue sections.

Different races and genders have unique skin and hair issues, requiring specialized care and more research for effective treatment.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Tofacitinib helped over half of the patients with severe hair loss regrow at least 50% of their hair.

Early intervention and tailored management can reduce skin side effects from cancer treatments.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Erosive pustular dermatosis in elderly people may be linked to aging immune systems and skin damage.

Dermoscopy can help assess the severity of chronic radiation-induced skin damage in head and neck cancer patients.

Pygmy goats with seborrhoeic dermatitis showed skin symptoms and temporary improvement with corticosteroids, but the cause and inheritance of the disease remain unknown.

A patient with multiple sclerosis developed skin reactions after Daclizumab treatment, requiring more data on the drug's effects.

MPZL3 is crucial for seborrheic dermatitis development.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

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.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Low zinc and selenium levels in sheep are linked to hair loss and thyroid problems.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Propolis and aloe vera ointment effectively treats mild to moderate psoriasis.

Scalp biopsies from dermatomyositis patients show chronic hair loss without scarring, with mucin and blood vessel changes being very common.