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Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Hair loss is linked to heart disease and metabolic syndrome, and while current treatments vary in effectiveness, more research is needed for better solutions.

Treating sheep and wild goats with specific medications and bathing sheep was 100% effective against a contagious skin disease caused by mites.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The document discussed hair loss causes and treatments but didn't give a final summary.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

White piedra is a rare hair infection treated with oral and topical antifungals.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

The growth of the Epstein-Barr virus in the patient's cells was linked to the worsening of her lymphoma.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Certain mature cells in mouse lungs can turn back into stem cells to aid in tissue repair.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

Intestinal stem cells can help repair skin damage from radiation.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

New models predict male pattern baldness better than old ones but still need improvement.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Melanocyte stem cells in hair follicles are key for hair color and could help treat greying and pigment disorders.