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Most patients with cutaneous lupus erythematosus in Bangladesh are young women, with chronic forms and photosensitivity being common.

Women with PCOS may have a higher risk of severe COVID-19 due to hormonal imbalances and vitamin D deficiency.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Cepharanthine analogues, especially tetrandrine, show potential for treating COVID-19.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

The COVID-19 pandemic increased the use of teledermatology to treat skin conditions in low-income areas, despite challenges like poor photo quality.

Severe COVID-19 often leads to hair loss in India.

Many COVID-19 survivors still face health issues months later, so ongoing medical support is important.

A patient with a rare chromosome condition also had a rare type of hair loss.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

People with chronic Hepatitis C often have skin problems like itching and contact dermatitis, especially older individuals and women.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Young Indians with coronary artery disease often have risk factors like smoking and central obesity, and cutaneous markers should be monitored for lifestyle changes.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Pregnancy can cause symptoms similar to rheumatic diseases, making diagnosis difficult, and affects various body systems, requiring careful distinction between normal changes and serious conditions.

COVID-19 may trigger hair loss conditions like alopecia areata.

The new skin-targeted COVID-19 vaccine creates strong immune responses and could improve vaccination methods.

Most pregnant women experience skin changes, with hyperpigmentation being the most common.

Switching flying squirrels' diet from seeds to mouse chow restored their hair.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Scalp fungus infections in Spain are a health concern, with changing causes and a need for better treatment and prevention.

Fever and rash can be early signs of lupus.

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Incorporating epidemic history into medical education is crucial to better address post-epidemic health challenges.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Ongoing monitoring and treatment are crucial to manage sarcoptic mange in reintroduced red foxes.

COVID-19 changed dermatology by increasing telemedicine and highlighting healthcare disparities.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A 9-year-old girl with a healthy immune system was successfully treated for a severe fungal scalp infection caused by Microsporum audouinii.