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Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Different hair loss types need accurate diagnosis for proper treatment.

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

Diuretics can cause serious side effects and should be used carefully.

Assessing newborn scalp hair can reveal important health information.

Growth factors and microneedle therapy increase hair density in women with hair loss.

Oral zinc sulphate reduces dark hair color in mice.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Removing lymph nodes does not improve survival for advanced ovarian cancer and may cause more complications.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Three natural compounds from Ghanaian plants may help treat BPH and alopecia.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Probiotics help reduce hair loss and increase hair growth in people with androgenic alopecia.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Prolactin affects hair growth and skin conditions, and could be a target for new skin disease treatments.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Many patients experience long-lasting symptoms like fatigue and pain after COVID-19, regardless of initial disease severity.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

The document concludes that understanding how adult stem and progenitor cells move is crucial for tissue repair and developing cell therapies.