Search

everythinglearnresearchcommunity

for

Search:↓

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.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

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

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.

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

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 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.

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.

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.

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Many displaced schoolchildren in Cameroon are malnourished, with high rates of thinness, stunting, underweight, and deficiencies in iron and protein.

Changes in gut bacteria can contribute to the development of Polycystic Ovary Syndrome (PCOS), affecting metabolism, immunity, and causing inflammation. Treatments may involve adjusting these factors.

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

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

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

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

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

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

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Solar drying is the best method for drying pomegranate peels quickly and efficiently.

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

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.