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A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

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.

Netherton Syndrome can cause severe skin lesions in rare cases.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

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

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Lipids may help treat hair loss by promoting hair growth.

5% topical minoxidil effectively treated a boy's congenital triangular alopecia without side effects.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Low-level light therapy, possibly combined with other treatments, may become a leading hair loss treatment, while hirsutism often worsens with age and lacks preventive options.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Fetal scalp cells have more regenerative genes than adult cells, and decellularized muscle matrix is better for muscle repair than commercial alternatives.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Adult hair follicle cells can create new hair follicles from corneal cells with the right support.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Children's skin diseases need special care and treatment.

Hair restoration techniques and new cell sources improve hair loss treatments.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

The document concludes that understanding the sebaceous gland's development and function is key to addressing related skin diseases and aging effects.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.