Search

everythinglearnresearchcommunity

for

Search:↓

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Trichotillometry is a reliable method to measure hair strength and assess hair loss treatments.

Skin doctors should recognize and treat conditions like hair-pulling and skin-picking early, often using therapy and medication, to help 50-70% of patients.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

Minoxidil treatment can stimulate hair growth in hairless puppies if applied early.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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

Targeting and modifying the stem cell niche can improve regenerative therapies.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Low-level laser therapy is safe and can increase hair growth for male and female pattern hair loss.

The document concludes that individualized treatments for hair issues are effective, certain hair changes can indicate neurocutaneous diseases, specific lotions improve skin health, laser hair removal works but needs more study on long-term effects, men's cosmetics are diverse, peeling is effective but can have side effects, and facial pigmentation is often due to overactive skin cells.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

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

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Photobiomodulation effectively treats hair loss in dogs with black hair follicular dysplasia.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

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

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

Recent progress has been made in understanding inherited hair and nail disorders.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.