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A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Dermoscopy greatly improves melanoma diagnosis and reduces unneeded surgeries.

Gendered social factors, not just biology, contribute to sex differences in adverse drug events.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

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.

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.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune 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.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Adding a second method to PROTACs could improve cancer treatment.

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.

Yellow and orange colors are important for diagnosing certain skin conditions.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

Detailed patient history and physical exams are crucial for diagnosing hair loss.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

The 11th AICPE Congress in Rimini was a major event in European aesthetic plastic surgery.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Interventional embolization is effective for treating scalp arteriovenous fistula but can cause complications like swelling and hair loss.

Alopecia Areata is a hair loss condition affecting all genders, often linked to other diseases, with treatments available but varying success rates.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Chronic Telogen Effluvium is a hair loss condition in middle-aged women that usually doesn't lead to complete baldness.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Light microscopy is useful for diagnosing different hair disorders.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Certain groups may need vitamin supplements to improve hair health and prevent other health problems.