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The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

A gene mutation causes woolly hair in a Syrian patient.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Minoxidil 2% effectively treats Monilethrix without side effects.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

Minoxidil promotes hair growth in male pattern baldness.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

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.

Eating vegetarian, having allergies, and family history might be linked to getting gray hair early.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

The document concludes that there is a need for more research and regulation in dermatology, covering topics like latex allergy in children, the use of botulinum toxin, and treatments for skin conditions.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

A 15-year-old girl has a benign skin tumor on her neck.

Nilotinib can cause keratosis pilaris, a skin condition.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

A specific gene mutation causes Olmsted syndrome.