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The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Targeted anticancer therapies can cause severe side effects similar to traditional chemotherapy, but with different types.

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.

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.

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 article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

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

A 25-year-old Malay fireman had skin bumps on his neck that were removed successfully after other treatments failed.

Epidermal nevi are skin cell clusters linked to various syndromes.

Eyelashes protect the eyes, but more research is needed to understand how.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

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

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Insulin resistance may contribute to various skin diseases and treating it could improve skin health and prevent more serious conditions.