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Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

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

Nanofat shows promise for facial rejuvenation and treating skin issues but needs more research for long-term safety.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Malassezia infection may cause refractory acne, and antifungal treatments can help.

IMA may indicate oxidative stress in skin and hair disorders, but more research is needed.

Cyclosporine-A can cause serious blood clots in the brain, so patients need careful monitoring.

High triglyceride levels are a key factor affecting testosterone levels in women with PCOS.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Neurotoxins can affect neurotransmitter release and have potential in treating muscle, pain, and cancer conditions, but more research is needed on how they work.

SCD1 inhibitors can cause skin issues in rodents.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

Regulatory T cells help heal skin and grow hair, and their absence can lead to healing issues and hair loss.

Ethnic Indian women with PCOS often have early symptoms, delayed diagnosis, and need better information and support for treatment and lifestyle management.

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

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Changes in gut bacteria can contribute to the development of Polycystic Ovary Syndrome (PCOS), affecting metabolism, immunity, and causing inflammation. Treatments may involve adjusting these factors.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Different PCOS types respond uniquely to infertility treatments, with some having lower pregnancy rates and higher risks of complications.

Early diagnosis and personalized treatment are crucial for managing PCOS and preventing complications.