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Chemotherapy can cause various skin problems, and recognizing them helps improve patient care.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Mice without Vitamin D receptors have hair growth problems because of issues in the hedgehog signaling pathway.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Eating the right nutrients can improve hair health, but taking extra supplements usually doesn't help unless you have a deficiency.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Light can turn on hair growth cells through a nerve path starting in the eyes.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Cortexolone 17a-propionate may be an effective new treatment for hair loss.

Detailed history and physical examination are crucial for diagnosing hair loss.

The article concludes that understanding the causes of hair loss and using continuous treatments like minoxidil and finasteride can help manage it, despite potential side effects.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Tigason improved hair growth in a boy with monilethrix without side effects.

Telogen effluvium is a reversible hair loss condition that requires a detailed diagnosis and often resolves on its own.

The document suggests using standardized methods to track and measure hair loss in alopecia areata, including patient self-assessment and a 50% improvement in specific scores as a treatment goal.

Hair loss in male pattern baldness involves muscle degeneration and increased scalp fat.

Telogen effluvium is a hair loss condition with acute cases resolving quickly and chronic cases potentially lasting longer, sometimes requiring treatment.

Men with common hair loss may have a higher risk of heart disease and diabetes, and should be checked for these conditions.

Permanent hair loss after bone marrow transplant can be caused by chemotherapy or chronic graft-versus-host disease.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.