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Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Genetically modifying a bacteria and changing its growth conditions significantly increased the production of a chemical called dipicolinic acid.

Methotrexate side effects vary by race and sex.

Topical 5-Fluorouracil can rarely cause nerve damage, especially in people with a certain genetic deficiency.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

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.

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

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Korean Red Ginseng has beneficial components that help with stress, immunity, fatigue, memory, blood flow, and disease protection.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Personalized treatment with inhibitors, minoxidil, and laser therapy helps hair loss.

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.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

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.

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 safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Four-amino acid part makes enzyme sensitive to finasteride.

EDA2R gene linked to hair loss.

Six new hair loss factors in men not linked to female hair loss.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.