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A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

A woman developed a skin condition called Pemphigus Vulgaris after a treatment to help with hair loss.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Adding aripiprazole to the treatment improved hair-pulling symptoms in a teenager.

A young woman had surgery to remove a large hairball that blocked her intestines and then got psychiatric help.

A man had severe stomach issues after a dental treatment with Formacresol, which improved with a different medication.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

An 86-year-old man had a rare tongue melanoma but refused treatment, showing the need for early cancer detection and treatment.

Most treatments for lichen planopilaris were found to be generally unsatisfactory.

An 84-year-old man developed severe anemia after his first COVID-19 vaccine shot, improved with treatment, and was advised against a second dose.

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.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

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.

Taking Propecia might lead to the development of cataracts.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

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.

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

Isotretinoin was not effective in treating facial lichen planopilaris.

Early diagnosis, intensive therapy, and careful follow-up are crucial for managing overlapping TTP and SLE.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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 2012 criteria are better for diagnosing atypical lupus cases.

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

Physical activity significantly improved symptoms of PCOS in a patient.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A woman's male-pattern facial hair growth was caused by a rare malignant ovarian tumor that was difficult to diagnose and treat.

COVID-19 may trigger or worsen rapid hair loss in alopecia areata.

Early diagnosis and treatment of systemic-onset juvenile idiopathic arthritis are crucial for improvement.