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Less than 10% of nursing students have PCOS, but many show symptoms and poor health habits, needing more education and yearly check-ups.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Iranian bodybuilders often use supplements like vitamins C, D, and whey protein, but they experience side effects like skin rashes and hair loss.

The hydrogel speeds up healing of infected wounds by providing oxygen and fighting bacteria.

Hydrogels show promise in preventing and treating skin damage from radiation therapy.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A patient with HAIR-AN syndrome, PCOS, and Hashimoto's thyroiditis improved with early diagnosis and treatment to prevent serious health problems.

Indian dermatosurgical practitioners were given guidelines in 2011 to reduce infection risks, including hand hygiene, sterilization methods, operation theater standards, and proper waste disposal.

Most hospitalized internal medicine patients have undiagnosed skin problems and want them treated.

A thorough skin history and full examination are important for diagnosing and understanding the impact of skin diseases.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Early diagnosis, genetic testing, and innovative treatments are crucial for managing complex medical conditions.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A community dermatology event in Delhi showed a high need for follow-up and awareness about skin conditions.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Awareness and better treatment of Demodex mites can improve health and quality of life.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Dystonia may be part of PAS-4 and linked to immune issues.

Vitamin D3 is important for bone health and may help treat various diseases beyond bone-related conditions.

The DNA convention was a valuable opportunity for learning and networking, especially after COVID-19.

DHT deficiency can disrupt cell connections in rat testes, possibly affecting fertility.

Early diagnosis and treatment of hair loss in hijab-wearing women are crucial to prevent permanent damage and improve quality of life.

Dupilumab can cause unexpected scalp issues, so early symptom recognition is important to avoid hair loss.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Patients with skin diseases rated psychological effects as most impactful, needing a treatment approach that addresses both mind and body.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

Skin issues can indicate immune system problems.