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Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Pediatric lichen is rare and diverse, and dermoscopy helps improve diagnosis and management in children.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Clascoterone cream effectively reduces acne severity and is safe for patients 12 and older.

A mutation in the Sgkl gene causes defective hair growth in mice.

The platform effectively grows lung cancer cell spheroids for drug testing.

Comprehensive genetic testing and international collaboration are crucial for better understanding and managing Ehlers-Danlos syndromes.

LC-OCT can help diagnose different types of scarring alopecia.

Increased EGFR gene variations may predict chemotherapy outcomes in small cell lung cancer patients.

Pincer nails are rare in lupus patients and may be managed conservatively.

A man with a rare scalp cancer was successfully treated, highlighting the need for early management to prevent spread and complications.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

A girl had two rare hair conditions that helped understand their overlap.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Children's Serum Sickness-Like Reaction is often linked to antibiotics, especially amoxicillin, and involves symptoms like rash, fever, and joint issues.

The International Society of Hair Restoration Surgery created a standard curriculum in 2008 to guide doctors in diagnosing and treating hair loss effectively.

Scientists can control how skin stem cells divide by using different treatments.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

Doctors should consider comedonic discoid lupus erythematosus to avoid misdiagnosis.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.