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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Curcumin may help reverse aging by targeting specific genes.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Hormones and genes affect hair growth and male baldness.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.