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Chronic lupus and frontal fibrosing alopecia can occur together, but their connection is unclear.

Brodalumab is more effective than ustekinumab in treating psoriasis.

Recognizing unusual symptoms can lead to early diagnosis and effective treatment of systemic lupus erythematosus.

Trichoscopy can help diagnose early congenital syphilis in newborns.

A new syndrome may link skin, growth, mental, and hair issues.

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 patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Technique effectively reconstructs large scalp defects with minimal hair loss and visible scarring.

The analyses helped identify different skin diseases in the two dogs.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

Special scalp and hair examination techniques can identify hair problems.

Ets2 gene is crucial for placental development in mice.

Nevus comedonicus can appear later in life and affect both eyelids.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The method effectively reduces and hides scalp defects after surgery.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

The boy's symptoms suggest a possible new medical condition.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.