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A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Cyproterone acetate can cause rare shortness of breath in women.

Severe digestive issues in DRESS need early endoscopy for better treatment.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

Proactive monitoring and management are essential to maximize the benefits of Trastuzumab Deruxtecan while minimizing serious side effects.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Hydroxychloroquine helped improve scleromyxoedema in patients, but caused side effects in some.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Best hair growth results from combining finasteride and minoxidil.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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.

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.

Taking Propecia might lead to the development of cataracts.

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.

Iron deficiency is not a significant cause of hair loss in women.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

The ShorT method can detect and help reduce bias in medical AI by identifying shortcut learning.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Minoxidil effectively lowers blood pressure with few side effects.

Hair loss can be linked to hormonal changes, and physical conditions like heart defects can cause depression.

A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

Using mesenchymal stem cells or their exosomes is safe for COVID-19 patients and helps improve lung healing and oxygen levels.

Many hospitalized children with COVID-19 had skin, mouth, or nail changes, with skin rashes being common.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

High-dose corticosteroid treatment helped improve symptoms in a patient with Adult Onset Still Disease.

Topical tofacitinib is effective and safe for treating alopecia areata.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.