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Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Thermoresponsive nanogels show promise for delivering medicine through the skin but need more safety testing and regulatory approval before clinical use.

Finasteride doesn't affect erections much, but may decrease libido in men.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Apoptosis may contribute to hair loss in androgenetic alopecia.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

Healthcare providers should start with simple fertility tests and treatments before referring patients to specialists.

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.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Telogen Effluvium is a hair loss condition where treatment involves identifying and managing its triggers.

A 28-year-old man with type 1 diabetes had skin and hair issues due to zinc deficiency.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.