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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

2-deoxy D-glucose does not help with hair regrowth in alopecia areata.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

Altered metabolism can help control seizures by changing brain signaling and energy use, suggesting new treatments for epilepsy.

The N gene affects the protein makeup of mouse hair.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.

Hair growth and pigmentation in mice involve specific stages crucial for research.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.

Modified KGF mRNA helps skin cells grow and move faster, which may improve wound healing.

Dermoscopy greatly improves melanoma diagnosis and reduces unneeded surgeries.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

Modified laparoscopic sleeve gastrectomy effectively controls diabetes and treats obesity with minimal complications.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Ovarian hyperthecosis can cause symptoms even with normal testosterone levels, and surgery can improve these symptoms.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

The ketogenic diet may help manage PCOS symptoms but needs more research for long-term effects.

Linagliptin slows down premature aging in certain mice.

A chubby child can still be malnourished.

The hydrogel speeds up diabetic wound healing by adapting to glucose levels and releasing insulin.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.

A misdiagnosed case of HAIR-AN syndrome led to unnecessary surgeries and highlighted the importance of correct diagnosis and treatment.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

Glibenclamide slows breast cancer cell growth by stopping cell division.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Monilethrix is linked to a gene cluster on chromosome 12.

Gestational diabetes increases risks for mothers and babies, needing early diagnosis and care.