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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.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Women with AGA have higher lipid levels, increasing heart disease risk.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

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.

A woman with scalp lymphoma and hair loss improved with radiotherapy, highlighting the need for biopsies in similar cases.

Puerto Rican children with cancer often experience symptoms like irritability, nausea, and hair loss, and need better education and continuous symptom management.

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

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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.

Wild geladas in crop areas show less grooming and aggression.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

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

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

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

Finasteride can cause muscle pain and high creatine kinase levels, but stopping the medication may resolve symptoms.

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.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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