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A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Pubic hair transplant surgery is an effective and permanent treatment for pubic hair loss.

Hair transplant surgery is a good cosmetic solution for people with little or no pubic hair, especially to boost their self-esteem.

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.

No CD44 in alopecia areata, present in normal and androgenetic alopecia.

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

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

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

CD2 might be a new treatment target for patchy alopecia areata.

A PET-CT scan successfully located a hard-to-find Leydig cell tumor in a woman with hormonal symptoms.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

Twins had rare skin cysts likely due to genetics.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

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

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Early diagnosis is crucial for treating alopecia effectively.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.