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Low-dose oral minoxidil effectively reduces hair loss in women with female pattern hair loss.

PCOS is a condition causing irregular periods, excess male hormones, and infertility, often managed by targeting insulin resistance and specific symptoms.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

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.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

Androgenetic alopecia is more common in Saudi men than women.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

A woman with severe hair loss was successfully treated with the drug adalimumab.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

The true incidence of post-Finasteride syndrome is unclear, and more research is needed.

Early diagnosis and a combination of treatments, including minoxidil and finasteride, are recommended for managing hair loss in India.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Injectable hydrogels are becoming increasingly useful in medicine for drug delivery and tissue repair.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

Menopause can cause hair thinning and texture changes due to hormonal and metabolic shifts.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.