Search

everythinglearnresearchcommunity

for

Search:↓

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

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Sp6 promotes tooth development by reducing follistatin levels.

People with Down's syndrome often have more skin problems due to a weak immune system.

Two gene areas linked to male pattern baldness found, more research needed.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Dutasteride is more efficient than finasteride, but individual results vary.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Finasteride may negatively affect male fertility.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

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.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

Researchers found a new mutation causing total hair loss from birth.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

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

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Low-dose finasteride may cause fertility issues, but stopping it can improve sperm quality and lead to pregnancy.

Gene differences may affect baldness treatment response in Korean men.

Finasteride shows promise for treating hair loss and excessive hair growth, but more research is needed to confirm its effectiveness and safety.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.