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Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Some anticonvulsant drugs can cause skin reactions, ranging from mild to severe, and managing these reactions is important for patient care.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Understanding and treating hair disorders in different ethnic groups requires knowledge of specific hair care practices and hair characteristics.

The new FDA labeling rules provide more detailed drug safety information for pregnant and breastfeeding women, but more data is needed on the risks of many dermatologic drugs.

The document concludes that more research is needed to understand and treat Beard Alopecia Areata due to limited current knowledge and evidence.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

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

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Egg shell membrane hydrolysates can reduce wrinkles and improve skin health.

Synthetic cannabinoid addiction can cause skin problems like acne and hair loss.

The position of the parietal whorl can predict safe donor areas for hair transplants in Korean men with male pattern baldness.

Canadian porcupines in a Japanese zoo passed a skin fungus to each other.

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

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Lack of cystatin M/E causes thin hair and dry skin.

Carboxytherapy can improve skin conditions with few side effects, but results may vary and are not guaranteed.

The critique suggests that Wilton's work unintentionally supports the very stereotypes it aims to question and calls for a broader, more inclusive approach to understanding gender.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The study could not confirm if Victor Vinnetou was Mbuyisa Makhubu and suggested more evidence, like DNA tests, is needed.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

Human hair varies widely and should be classified by curl type rather than race.

Feeling shame can make it harder for people with diabetes to take care of their health.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Children with autoimmune gastritis showed improved intestinal health over time and should be checked for other autoimmune conditions.

Increasing olanzapine caused hair loss in a woman, which stopped after changing medication.

Injections with 0.5% minoxidil effectively treat female hair loss, increasing hair density and thickness.