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The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

FGF-1 causes spiral ganglion neurites to branch more.

Hairless gene not strongly linked to baldness.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Cantú syndrome may be linked to pituitary adenomas.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.