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Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Neurons from hair follicles can help repair damaged nerves.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Cell proteomic footprinting enhances cancer vaccine quality by ensuring correct antigen composition.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

ECCL should be considered in patients with specific skin and eye lesions.

Transfected cells with VEGF and FGF2 genes improve skin wound healing by enhancing blood flow and regeneration.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Non-coding RNAs help control hair growth in cashmere goats.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A rare benign scalp tumor in an infant requires surgical removal.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Nestin-expressing hair follicle cells may be useful for nerve repair and regeneration.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Patients with graft-versus-host disease often have nail changes related to the nail matrix, with severity not linked to skin condition.

TCM-derived nanovesicles show promise for wound healing and skin regeneration but need more research.

Capivasertib improves survival in certain breast cancer cases but requires careful management of side effects.

Engineered extracellular vesicles could improve CRISPR/Cas delivery, making gene editing safer and more effective.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Twins had rare skin cysts likely due to genetics.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.