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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.

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.

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.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Understanding skin structure and development helps diagnose and treat skin disorders.

Nitroglycerin ointment is now used to treat several skin conditions with fewer side effects.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

The document concludes that each reviewed medical book is useful for its specific area in pediatric care, especially the "Neonatal Formulary" for neonatal drug information.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Wnt signaling is crucial for skin and hair development and its disruption can cause skin tumors.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

Tattooing helps treat skin conditions, reconstruct nipple-areola, mark radiation fields, and locate lesions.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

New treatments for a chronic skin condition show promise, but individualized plans are crucial due to varying responses.