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A gene called HDAC9 might be a new factor in male-pattern baldness.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

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

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

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

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

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

Chinese patients with systemic lupus erythematosus commonly experience oral ulcers, arthritis, alopecia, skin rash, and nephritis.

Immune checkpoint inhibitors can cause skin issues but are linked to better cancer outcomes.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Women with lichen planopilaris often have thyroid disease, depression, anxiety, and may respond to treatment with slowed disease progression.

New protein changes may be involved in the immune attack on hair follicles in alopecia areata.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variations increase the risk of alopecia areata in Koreans.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Two siblings both had a rare case of alopecia areata at the same time.

A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.