Search

everythinglearnresearchcommunity

for

Search:↓

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Androgenetic alopecia is influenced by various factors and can be treated with medications, procedures, and non-drug methods.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Certain genes may influence hair loss differently in men and women.

Alopecia areata patients, especially women with nail issues or atopic diseases, are at higher risk for other autoimmune diseases.

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

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A new gene mutation causes insulin resistance in a girl and her mother.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Certain gene variations may increase the risk and severity of alopecia areata.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Blocking the enzyme 5α-reductase can shrink the prostate and help treat enlarged prostate issues.

Androgens can both increase and decrease hair growth in different parts of the body.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Amenorrhea is relatively rare and initial testing should check FSH, TSH, and prolactin levels.

New genes and pathways are important for testosterone production and male sexual development.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

High levels of androgens during early development may cause PCOS-like symptoms.