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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

New cell-based therapies may improve hair loss treatments in the future.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

Eicosanoids are crucial for skin health, and targeting their pathways may help treat skin conditions.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Lack of cystatin M/E causes thin hair and dry skin.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Hirsutism is often caused by high male hormone levels and can be treated with lifestyle changes and medications.

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

Effective hirsutism management requires identifying the cause, combining new and traditional treatments, and setting realistic expectations for patients.

Skin issues can indicate immune system problems.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

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.