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Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

Some women with PCOS have rare genetic variants linked to the condition.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

Biotin supplements significantly improved a young girl's uncombable hair.

Ocrelizumab may cause total body hair loss in some patients.

A skin model using hair and skin cells can mimic human skin for research.

A simple screening method found that 6.3% of women in a semiurban area in Sri Lanka have polycystic ovary syndrome, with most showing menstrual irregularities.

Gene expression affects fur development in rex rabbits.

Lack of Evi in skin causes psoriasis-like symptoms in mice.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

The woman has scurvy and needs more vitamin C.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

UVB exposure affects retinoid metabolism, which is important for skin cancer progression and treatment.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

New ultrasound criteria for diagnosing PCOS in North African patients were successfully established.

The new hair graft device is faster, more efficient, and reduces damage to hair follicles.

UC-MSC-Es help human hair cells grow.

Msx2 deficiency in mice leads to bone growth and organ development problems.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

A special blood test helped find the overactive ovary in a teen with PCOS, and removing that ovary improved her condition.

Regulating keratinocyte growth in engineered skin can improve wound healing.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Human hair protein patterns are inherited genetically.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.