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Higher levels of retinol-binding protein 4 are found in people with alopecia areata, but these levels don't relate to how severe the condition is.

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

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Plucked hair follicles can help diagnose scalp lupus.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

Two peptides, RMYYY and VMYMI, may be effective anti-inflammatory drugs.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

Ritlecitinib is effective for long-term treatment of severe alopecia areata.

Effective monitoring and prevention strategies are needed to manage the spread of hand, foot, and mouth disease in children.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

Rezpegaldesleukin shows promise for treating severe alopecia areata.

A woman with lupus had blood cell destruction, treated successfully with medication.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

Ritlecitinib effectively treats alopecia areata and is safe for long-term use in people 12 and older.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.